Phosphoric benzoyl derivatives and their use as herbicides

ABSTRACT

Phosphorus-containing benzoyl derivatives of the formula I                    
     where: 
     P(═X)R 1 R 2 X is an organic phosphorus radical; 
     R 3  is hydrogen, nitro, cyano, halogen, unsub. or sub. alkyl, alkylcarbonyl, alkoxycarbonyl, unsub. or sub. alkoxy, unsub. or sub. alkylthio, unsub. or sub. alkylsulfinyl, unsub. or sub. alkylsulfonyl, unsub. or sub. aminosulfonyl, unsub. or sub. amino, P(═X)R 1 R 2 , unsub. or sub. phenyl or unsub. or sub. heterocyclyl; 
     R 4  is nitro, cyano, halogen, alkyl, alkoxy, alkylthio, alkylsulfinyl or alkylsulfonyl; 
     l is 0, 1 or 2; 
     Q is unsub. or sub. 1-hydroxy-3-oxocyclohex-1-en-2-yl, unsub. or sub. 5-hydroxypyrazol-4-yl, unsub. or sub. isoxazol-4-yl or unsub. or sub. 2-cyano-1-oxoeth-2-yl; 
     and their agriculturally useful salts; 
     processes and intermediates for preparing the phosphorus-containing benzoyl derivatives; compositions comprising them and the use of these derivatives or the compositions comprising them for controlling undesirable plants are described.

This application is a 371 of PCT/EP00/03548 Apr. 19, 2000.

The present invention relates to phosphorus-containing benzoyl derivatives of the formula I

in which:

X is oxygen or sulfur;

R¹,R² are hydrogen, C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl, hydroxyl, C₁-C₆-alkoxy, C₃-C₆-alkenyloxy, C₃-C₆-alkynyloxy, mercapto, C₁-C₆-alkylthio, C₃-C₆-alkenylthio, C₃-C₆-alkynylthio, amino, C₁-C₆-alkylamino, di(C₁-C₆-alkyl)amino, (C₁-C₆-alkoxy)(C₁-C₆-alkyl)amino, (C₃-C₆-alkenyl)(C₁-C₆-alkyl)amino, (C₃-C₆-alkynyl)(C₁-C₆-alkyl)amino, di(C₃-C₆-alkenyl)amino or di(C₃-C₆-alkynyl)amino, where the abovementioned alkyl, alkenyl or alkynyl radicals may be partially or fully halogenated and/or may carry one to three of the following groups: nitro, cyano, C₁-C₄-alkoxy, C₁-C₄-alkylthio, C₁-C₄-alkylsulfinyl, C₁-C₄-alkylsulfonyl, di(C₁-C₄-alkyl)amino, C₁-C₄-alkylcarbonyl, C₁-C₄-alkoxycarbonyl, phenyl or heterocyclyl, where the the two last-mentioned radicals for their part may be partially or fully halogenated and/or may carry one to three of the following groups:

nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy or C₁-C₄-alkoxycarbonyl;

 are phenyl or phenoxy which may be partially or fully halogenated and/or may carry one to three of the following groups:

nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy or C₁-C₄-alkoxycarbonyl; or

R¹ and R² together form an —O—(CH₂)_(m)—O—, —O—(CH₂)_(m)—S—, —S—(CH₂)_(m)—S—, —NR⁵—(CH₂)_(m)—NR⁵—, —O—(CH₂)_(m)—NR⁵—, —S—(CH₂)_(m)—NR⁵—, —(CH₂)_(n)—O—, —(CH₂)_(n)—S— or —(CH₂)_(n)—NR⁵ chain which may carry one to three radicals from the following group:

halogen, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-alkoxycarbonyl or phenyl which is unsubstituted or partially or fully halogenated and/or may carry one to three of the following groups:

nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy or C₁-C₄-alkoxycarbonyl; or

R¹ and R² together form a —(CH₂)_(p) chain which may be interrupted by oxygen, sulfur or NR⁵ and/or may carry one to three radicals from the following group:

halogen, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-alkoxycarbonyl or phenyl which is unsubstituted or partially or fully halogenated and/or may carry one to three of the following groups: nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy or C₁-C₄-alkoxycarbonyl;

R³ is hydrogen, nitro, cyano, halogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy-C₁-C₆-alkyl, C₁-C₆-haloalkoxy-C₁-C₆-alkyl, C₁-C₆-alkylthio-C₁-C₆-alkyl, C₁-C₆-alkylsulfinyl-C₁-C₆-alkyl, C₁-C₆-alkylsulfonyl-C₁-C₆-alkyl, C₁-C₆-alkylcarbonyl, C₁-C₆-alkoxycarbonyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₁-C₆-alkylthio, C₁-C₆-haloalkylthio, C₁-C₆-alkylsulfinyl, C₁-C₆-haloalkylsulfinyl, C₁-C₆-alkylsulfonyl, C₁-C₆-haloalkylsulfonyl, aminosulfonyl, C₁-C₆-alkylaminosulfonyl, di(C₁-C₆-alkyl)aminosulfonyl, (C₁-C₆-alkylsulfonyl)amino, (C₁-C₆-haloalkylsulfonyl)amino, N—(C₁-C₆-alkyl)—N—(C₁-C₆-alkylsulfonyl)amino, N—(C₁-C₆-alkyl)—N—(C₁-C₆-haloalkylsulfonyl)amino, —P(═X)R¹R², phenyl or heterocyclyl, where the two last-mentioned radicals may be partially or fully halogenated and/or may carry one to three of the following groups:

nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy or C₁-C₄-alkoxycarbonyl;

R⁴ is nitro, cyano, halogen, C₁-C₆-alkyl, C₁-C₆-alkoxy, C₁-C₆-alkylthio, C₁-C₆-alkylsulfinyl or C₁-C₆-alkylsulfonyl;

R⁵ is hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl or C₁-C₆-alkoxy;

l is 0, 1 or 2;

m is 2, 3 or 4;

n is 3, 4 or 5;

p is 4, 5 or 6;

Q is a radical of the formula Q¹, Q², Q³ or Q⁴

R⁶ is hydroxyl, mercapto, halogen, OR¹³, SR¹³, SOR¹⁴, SO₂R¹⁴, OSO₂R¹⁴, POR¹⁵R¹⁶, OPR¹⁵R¹⁶, OPOR¹⁵R¹⁶, OPSR¹⁵R¹⁶, NR¹⁷R¹⁸, ONR¹⁸R¹⁹, N-bonded heterocyclyl or O—(N-bonded heterocyclyl), where the heterocyclyl radical of the two last-mentioned substituents may be partially or fully halogenated and/or may carry one to three of the following radicals:

nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy or C₁-C₄-haloalkoxy;

R⁷,R⁹,R¹¹ are hydrogen, nitro, halogen, cyano, C₁-C₆-alkyl, C₁-C₆-haloalkyl, di(C₁-C₆-alkoxy)methyl, di(C₁-C₆-alkylthio)methyl, (C₁-C₆-alkoxy)(C₁-C₆-alkylthio)methyl, hydroxyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₁-C₆-alkoxycarbonyloxy, C₁-C₆-alkylthio, C₁-C₆-haloalkylthio, C₁-C₆-alkylsulfinyl, C₁-C₆-haloalkylsulfinyl, C₁-C₆-alkylsulfonyl, C₁-C₆-haloalkylsulfonyl, C₁-C₆-alkylcarbonyl, C₁-C₆-haloalkylcarbonyl, C₁-C₆-alkoxycarbonyl or C₁-C₆-haloalkoxycarbonyl;

R⁸,R¹⁰,R¹² are hydrogen, C₁-C₆-alkyl, C₁-C₆-alkoxy, C₁-C₆-alkylthio or C₁-C₆-alkoxycarbonyl; or

R⁷ and R⁸ or R⁹ and R¹⁰ or R¹¹ and R¹² together form an —O—(CH₂)_(u)—O—, —O—(CH₂)_(u)—S—, —S—(CH₂)_(u)—S—, —O—(CH₂)_(v)— or —S—(CH₂)_(v) chain which may be substituted by one to three radicals from the following group:

halogen, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl or C₁-C₄-alkoxycarbonyl; or

R⁷ and R⁸ or R⁹ and R¹⁰ or R¹¹ and R¹² together form a —(CH₂)_(w) chain which may be interrupted by oxygen or sulfur and/or may be substituted by one to four radicals from the following group:

halogen, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl or C₁-C₄-alkoxycarbonyl; or

R⁷ and R⁸ or R⁹ and R¹⁰ or R¹¹ and R¹² together form a methylidene group which may be substituted by one to two radicals from the following group:

halogen, hydroxyl, formyl, cyano, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₁-C₆-alkylthio, C₁-C₆-haloalkylthio, C₁-C₆-alkylsulfinyl, C₁-C₆-haloalkylsulfinyl, C₁-C₆-alkylsulfonyl or C₁-C₆-haloalkylsulfonyl; or

R⁷ and R⁸ or R⁹ and R¹⁰ or R¹¹ and R¹² together with the carbon atom to which they are attached form a carbonyl group; or

R⁷ and R⁹ or R⁹ and R¹¹ or R⁷ and R¹¹ together form a —(CH₂)_(v) chain which may be substituted by one to three radicals from the following group:

halogen, C₁-C₆-alkyl, C₁-C₆-alkoxy, hydroxyl or C₁-C₆-alkoxycarbonyl;

R¹³ is C₁-C₆-alkyl, C₃-C₆-alkenyl, C₃-C₆-haloalkenyl, C₃-C₆-alkynyl, C₃-C₆-haloalkynyl, C₃-C₆-cycloalkyl, C₁-C₂₀-alkylcarbonyl, C₂-C₆-alkenylcarbonyl, C₂-C₆-alkynylcarbonyl, C₃-C₆-cycloalkylcarbonyl, C₁-C₆-alkylaminocarbonyl, C₁-C₆-alkylcarbonyl-C₁-C₆-alkyl or C₁-C₆-alkoxyimino-C₁-C₆-alkyl, where the abovementioned alkyl and cycloalkyl radicals may be partially or fully halogenated and/or may carry one to three of the following groups:

cyano, C₁-C₄-alkoxy, C₁-C₄-alkylthio, di(C₁-C₄-alkyl)amino, C₁-C₄-alkylcarbonyl, C₁-C₄-alkoxycarbonyl, C₁-C₄-alkoxy-C₁-C₄-alkoxycarbonyl, di(C₁-C₄-alkyl)amino-C₁-C₄-alkoxycarbonyl, hydroxycarbonyl, C₁-C₄-alkylaminocarbonyl, di(C₁-C₄-alkyl)aminocarbonyl, aminocarbonyl, C₁-C₄-alkylcarbonyloxy or C₃-C₆-cycloalkyl;

is phenyl, heterocyclyl, phenyl-C₁-C₆-alkyl, heterocyclyl-C₁-C₆-alkyl, phenylcarbonyl, heterocyclylcarbonyl, phenylaminocarbonyl or heterocyclylaminocarbonyl, where the phenyl and the heterocyclyl radical of the 8 last-mentioned substituents may be partially or fully halogenated and/or may carry one to three of the following radicals:

nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy or C₁-C₄-haloalkoxy;

R¹⁴,R¹⁵, R¹⁶ are C₁-C₆-alkyl, C₃-C₆-alkenyl, C₃-C₆-haloalkenyl, C₃-C₆-alkynyl, C₃-C₆-haloalkynyl, C₃-C₆-cycloalkyl, hydroxyl, C₁-C₆-alkoxy, amino, C₁-C₆-alkylamino, C₁-C₆-haloalkylamino, di(C₁-C₆-alkyl)amino or di(C₁-C₆-haloalkyl)amino, where the abovementioned alkyl, cycloalkyl and alkoxy radicals may be partially or fully halogenated and/or may carry one to three of the following groups:

cyano, C₁-C₄-alkoxy, C₁-C₄-alkylthio, di(C₁-C₄-alkyl)amino, C₁-C₄-alkylcarbonyl or C₁-C₄-alkoxycarbonyl;

are phenyl, heterocyclyl, phenoxy or heterocyclyloxy, where the phenyl and the heterocyclyl radical of the last-mentioned substituents may be partially or fully halogenated and/or may carry one to three of the following radicals:

nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy or C₁-C₄-haloalkoxy;

R¹⁷ is C₁-C₆-alkyl, C₃-C₆-alkenyl, C₃-C₆-haloalkenyl, C₃-C₆-alkynyl, C₃-C₆-halogenalkynyl, C₃-C₆-cycloalkyl, hydroxyl, C₁-C₆-alkoxy, C₃-C₆-alkenyloxy or C₃-C₆-alkynyloxy, where the abovementioned alkyl, cycloalkyl and alkoxy radicals may be partially or fully halogenated and/or may carry one to three radicals from the following groups:

cyano, C₁-C₄-alkoxy, C₁-C₄-alkylthio or di(C₁-C₄-alkyl)amino;

is phenyl, heterocyclyl, phenyl-C₁-C₆-alkyl or heterocyclyl-C₁-C₆-alkyl, where the phenyl or heterocyclyl radical of the four last-mentioned substituents may be partially or fully halogenated and/or may carry one to three of the following radicals:

nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy or C₁-C₄-haloalkoxy;

R¹⁸, R¹⁹ are C₁-C₆-alkyl, C₃-C₆-alkenyl, C₃-C₆-alkynyl or C₁-C₆-alkylcarbonyl;

u is 2 to 4;

v is 1 to 5;

w is 2 to 5;

R²⁰ is a radical as mentioned under R⁶;

R²¹ is hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl, hydroxyl, C₁-C₆-alkoxy or C₁-C₆-haloalkoxy;

R²² is hydrogen, halogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl, hydroxyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₁-C₆-alkylthio or C₁-C₆-haloalkylthio;

R²³ is hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₃-C₆-cycloalkyl or C₃-C₆-halocycloalkyl;

R²⁴ is hydrogen, C₁-C₆-alkoxycarbonyl, C₁-C₆-haloalkoxycarbonyl, hydroxycarbonyl or cyano;

R²⁵ is C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₃-C₆-cycloalkyl or C₃-C₆-halocycloalkyl;

and their agriculturally useful salts.

Moreover, the invention relates to the processes and intermediates for preparing compounds of the formula I, compositions comprising them and to the use of the compounds of the formula I and of the compositions comprising them for controlling pests.

Herbicidally effective phosphorothionoamidates are disclosed in the literature, for example in DE-A 22 60 705 and DE-A 21 66 729. Furtheermore, U.S. Pat. No. 3,775,057 describes pyridinylphosphonates.

Likewise, substituted benzoylisoxazoles or -pyrazoles and substituted 2-phenylcyclohexane-1,3-diones or 1-phenyl-2-cyanoalkane-1,3-diones are disclosed, for example, in EP-A 418 175, EP-A 609 797, WO 96/26 192, WO 96/26 206, EP-A 203 428, U.S. Pat. No. 4,780,127, EP-A 315 075 and EP-A 625 505.

However, the herbicidal properties of the prior art compounds and their compatibility with crop plants are not entirely satisfactory. It is an object of the present invention to provide novel, in particular herbicidally effective compounds having improved properties.

We have found that this object is achieved by the phosphorus-containing benzoyl derivatives of the formula I and their herbicidal action.

Furthermore, we have found herbicidal compositions comprising the compounds I and having very good herbicidal action. Moreover, we have found processes for preparing these compositions and methods for controlling undesirable vegetation using the compounds I.

Depending on the substitution pattern, the compounds of the formula I can contain one or more chiral centers, in which case they exist in the form of enantiomers or diastereomer mixtures.

The invention provides both the pure enantiomers or diastereomers and mixtures thereof.

The compounds of the formula I can also be present in the form of their agriculturally useful salts, the type of salt generally being immaterial. In general, the salts of those cations or the acid addition salts of those acids are suitable whose cations and anions, respectively, do not affect the herbicidal action of the compounds I negatively.

Suitable cations are, in particular, ions of the alkali metals, preferably lithium, sodium and potassium, the alkaline earth metals, preferably calcium and magnesium, and the transition metals, preferably manganese, copper, zinc and iron, and also ammonium, where, if desired, one to four hydrogen atoms may be replaced by C₁-C₄-alkyl, hydroxy-C₁-C₄-alkyl, C₁-C₄-alkoxy-C₁-C₄-alkyl, hydroxy-C₁-C₄-alkoxy-C₁-C₄-alkyl, phenyl or benzyl, preferably ammonium, dimethylammonium, diisopropylammonium, tetramethylammonium, tetrabutylammonium, 2-(2-hydroxyeth-1-oxy)eth-1-ylammonium, di(2-hydroxyeth-1-yl)ammonium, trimethylbenzylammonium, furthermore phosphonium ions, sulfonium ions, preferably tri(C₁-C₄-alkyl)sulfonium and sulfoxonium ions, preferably tri(C₁-C₄-alkyl)sulfoxonium.

Anions of useful acid addition salts are primarily chloride, bromide, fluoride, hydrogen sulfate, sulfate, dihydrogen phosphate, hydrogen phosphate, nitrate, hydrogen carbonate, carbonate, hexafluorosilicate, hexafluorophosphate, benzoate and the anions of C₁-C₄-alkanoic acids, preferably formate, acetate, propionate and butyrate.

The organic molecular moieties mentioned for the substituents R¹-R²⁵ or as radicals on phenyl and heterocyclyl radicals are collective terms for individual lists of the individual group members. All hydrocarbon chains, i.e. all alkyl, haloalkyl, alkoxy, haloalkoxy, alkylthio, haloalkylthio, alkylsulfinyl, haloalkylsulfinyl, alkylsulfonyl, haloalkylsulfonyl, alkylaminosulfonyl, dialkylaminosulfonyl, alkylamino, dialkylamino, haloalkylamino, di(haloalkyl)amino, N-alkoxy-N-alkylamino, N-alkylsulfonylamino, N-haloalkylsulfonylamino, N-alkyl-N-alkylsulfonylamino, N-alkyl-N-haloalkylsulfonylamino, alkylcarbonyl, haloalkylcarbonyl, alkoxycarbonyl, haloalkoxycarbonyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkoxyalkyl, haloalkoxyalkyl, alkylthioalkyl, alkylsulfinylalkyl, alkylsulfonylalkyl, dialkoxymethyl, dialkylthiomethyl, (alkoxy)(alkylthio)methyl, alkylcarbonylalkyl, alkoxyiminoalkyl, alkoxycarbonyloxy, phenylalkyl, heterocyclylalkyl, dialkylaminoalkoxycarbonyl, alkoxyalkoxycarbonyl, alkenylcarbonyl, N-alkenyl-N-alkylamino, dialkenylamino, alkynylcarbonyl, N-alkynyl-N-alkylamino, dialkynylamino, alkenyl, alkynyl, haloalkenyl, haloalkynyl, alkenyloxy, alkenylthio, alkynyloxy and alkynylthio moieties can be straight-chain or branched. Unless indicated otherwise, halogenated substituents preferably carry one to five identical or different halogen atoms. The term halogen represents in each case fluorine, chlorine, bromine or iodine.

Examples of other meanings are:

C₁-C₄-alkyl: for example methyl, ethyl, propyl, 1-methylethyl, butyl, 1-methylpropyl, 2-methylpropyl or 1,1-dimethylethyl;

C₁-C₆-alkyl, and the alkyl moieties of C₁-C₆-alkylcarbonyl-C₁-C₆-alkyl, C₁-C₆-alkoxyimino-C₁-C₆-alkyl, N—(C₃-C₆-alkenyl)-N—(C₁-C₆-alkyl)amino, N—(C₃-C₆-alkynyl)-N—(C₁-C₆-alkyl)amino, phenyl-C₁-C₆-alkyl, N—(C₁-C₆-alkyl)-N—(C₁-C₆-alkylsulfonyl)amino, N—(C₁-C₆-alkyl)-N—(C₁-C₆-haloalkylsulfonyl)amino, heterocyclyl-C₁-C₆-alkyl: C₁-C₄-alkyl as mentioned above, and also, for example, pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 2,2-dimethylpropyl, 1-ethylpropyl, hexyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, 1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1,1-dimethylbutyl, 1,2-dimethylbutyl, 1,3-dimethylbutyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl, 1-ethylbutyl, 2-ethylbutyl, 1,1,2-trimethylpropyl, 1-ethyl-1-methylpropyl or 1-ethyl-3-methylpropyl;

C₁-C₄-haloalkyl: a C₁-C₄-alkyl radical as mentioned above which is partially or fully substituted by fluorine, chlorine, bromine and/or iodine, i.e., for example, chloromethyl, dichloromethyl, trichloromethyl, fluoromethyl, difluoromethyl, trifluoromethyl, chlorofluorpmethyl, dichlorofluoromethyl, chlorodifluoromethyl, 2-fluoroethyl, 2-chloroethyl, 2-bromoethyl, 2-iodoethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl, 2-chloro-2-fluoroethyl, 2-chloro-2,2-difluoroethyl, 2,2-dichloro-2-fluoroethyl, 2,2,2-trichloroethyl, pentafluoroethyl, 2-fluoropropyl, 3-fluoropropyl, 2,2-difluoropropyl, 2,3-difluoropropyl, 2-chloropropyl, 3-chloropropyl, 2,3-dichloropropyl, 2-bromopropyl, 3-bromopropyl, 3,3,3-trifluoropropyl, 3,3,3-trichloropropyl, 2,2,3,3,3-pentafluoropropyl, heptafluoropropyl, 1-(fluoromethyl)-2-fluoroethyl, 1-(chloromethyl)-2-chloroethyl, 1-(bromomethyl)-2-bromoethyl, 4-fluorobutyl, 4-chlorobutyl, 4-bromobutyl or nonafluorobutyl;

C₁-C₆-haloalkyl, and the haloalkyl moieties of C₁-C₆-haloalkylamino, di(C₁-C₆-haloalkyl)amino: C₁-C₄-haloalkyl, as mentioned above, and also, for example, 5-fluoropentyl, 5-chloropentyl, 5-bromopentyl, 5-iodopentyl, undecafluoropentyl, 6-fluorohexyl, 6-chlorohexyl, 6-bromohexyl, 6-iodohexyl or dodecafluorohexyl;

C₁-C₄-alkoxy: for example methoxy, ethoxy, propoxy, 1-methylethoxy, butoxy, 1-methylpropoxy, 2-methylpropoxy or 1,1-dimethylethoxy;

C₁-C₆-alkoxy, and the alkoxy moieties of di(C₁-C₆-alkoxy)methyl, (C₁-C₆-alkoxy)(C₁-C₆-alkylthio)methyl, C₁-C₆-alkoxyimino-C₁-C₆-alkyl and N—(C₁-C₆-alkoxy)-N—(C₁-C₆-alkyl)amino: C₁-C₄-alkoxy as mentioned above, and also, for example, pentoxy, 1-methylbutoxy, 2-methylbutoxy, 3-methylbutoxy, 1,1-dimethylpropoxy, 1,2-dimethylpropoxy, 2,2-dimethylpropoxy, 1-ethylpropoxy, hexoxy, 1-methylpentoxy, 2-methylpentoxy, 3-methylpentoxy, 4-methylpentoxy, 1,1-dimethylbutoxy, 1,2-dimethylbutoxy, 1,3-dimethylbutoxy, 2,2-dimethylbutoxy, 2,3-dimethylbutoxy, 3,3-dimethylbutoxy, 1-ethylbutoxy, 2-ethylbutoxy, 1,1,2-trimethylpropoxy, 1,2,2-trimethylpropoxy, 1-ethyl-1-methylpropoxy or 1-ethyl-2-methylpropoxy;

C₁-C₄-haloalkoxy: a C₁-C₄-alkoxy radical as mentioned above which is partially or fully substituted by fluorine, chlorine, bromine and/or iodine, i.e., for example, fluoromethoxy, difluoromethoxy, trifluoromethoxy, chlorodifluoromethoxy, bromodifluoromethoxy, 2-fluoroethoxy, 2-chloroethoxy, 2-bromomethoxy, 2-iodoethoxy, 2,2-difluoroethoxy, 2,2,2-trifluoroethoxy, 2-chloro-2-fluoroethoxy, 2-chloro-2,2-difluoroethoxy, 2,2-dichloro-2-fluoroethoxy, 2,2,2-trichloroethoxy, pentafluoroethoxy, 2-fluoropropoxy, 3-fluoropropoxy, 2-chloropropoxy, 3-chloropropoxy, 2-bromopropoxy, 3-bromopropoxy, 2,2-difluoropropoxy, 2,3-difluoropropoxy, 2,3-dichloropropoxy, 3,3,3-trifluoropropoxy, 3,3,3-trichloropropoxy, 2,2,3,3,3-pentafluoropropoxy, heptafluoropropoxy, 1-(fluoromethyl)-2-fluoroethoxy, 1-(chloromethyl)-2-chloroethoxy, 1-(bromomethyl)-2-bromoethoxy, 4-fluorobutoxy, 4-chlorobutoxy, 4-bromobutoxy or nonafluorobutoxy;

C₁-C₆-haloalkoxy, and the haloalkoxy moieties of C₁-C₆-haloalkoxy-C₁-C₆-alkyl: C₁-C₄-haloalkoxy as mentioned above, and also, for example, 5-fluoropentoxy, 5-chloropentoxy, 5-bromopentoxy, 5-iodopentoxy, undecafluoropentoxy, 6-fluorohexoxy, 6-chlorohexoxy, 6-bromohexoxy, 6-iodohexoxy or dodecafluorohexoxy;

C₁-C₄-alkylthio: for example methylthio, ethylthio, propylthio, 1-methylethylthio, butylthio, 1-methylpropylthio, 2-methylpropylthio or 1,1-dimethylethylthio;

C₁-C₆-alkylthio, and the alkylthio moieties of C₁-C₆-alkylthio-C₁-C₆-alkyl, di(C₁-C₆-alkylthio)methyl and (C₁-C₆-alkoxy)(C₁-C₆-alkylthio)methyl: C₁-C₄-alkylthio as mentioned above, and also, for example, pentylthio, 1-methylbutylthio, 2-methylbutylthio, 3-methylbutylthio, 2,2-dimethylpropylthio, 1-ethylpropylthio, hexylthio, 1,1-dimethylpropylthio, 1,2-dimethylpropylthio, 1-methylpentylthio, 2-methylpentylthio, 3-methylpentylthio, 4-methylpentylthio, 1,1-dimethylbutylthio, 1,2-dimethylbutylthio, 1,3-dimethylbutylthio, 2,2-dimethylbutylthio, 2,3-dimethylbutylthio, 3,3-dimethylbutylthio, 1-ethylbutylthio, 2-ethylbutylthio, 1,1,2-trimethylpropylthio, 1,2,2-trimethylpropylthio, 1-ethyl-1-methylpropylthio or 1-ethyl-2-methylpropylthio;

C₁-C₆-haloalkylthio: a C₁-C₆-alkylthio radical as mentioned above which is partially or fully substituted by fluorine, chlorine, bromine and/or iodine, i.e., for example, fluoromethylthio, difluoromethylthio, trifluoromethylthio, chlorodifluoromethylthio, bromodifluoromethylthio, 2-fluoroethylthio, 2-chloroethylthio, 2-bromoethylthio, 2-iodoethylthio, 2,2-difluoroethylthio, 2,2,2-trifluoroethylthio, 2,2,2-trichloroethylthio, 2-chloro-2-fluoroethylthio, 2-chloro-2,2-difluoroethylthio, 2,2-dichloro-2-fluoroethylthio, pentafluoroethylthio, 2-fluoropropylthio, 3-fluoropropylthio, 2-chloropropylthio, 3-chloropropylthio, 2-bromopropylthio, 3-bromopropylthio, 2,2-difluoropropylthio, 2,3-difluoropropylthio, 2,3-dichloropropylthio, 3,3,3-trifluoropropylthio, 3,3,3-trichloropropylthio, 2,2,3,3,3-pentafluoropropylthio, heptafluoropropylthio, 1-(fluoromethyl)-2-fluoroethylthio, 1-(chloromethyl)-2-chloroethylthio, 1-(bromomethyl)-2-bromoethylthio, 4-fluorobutylthio, 4-chlorobutylthio, 4-bromobutylthio, nonafluorobutylthio, 5-fluoropentylthio, 5-chloropentylthio, 5-bromopentylthio, 5-iodopentylthio, undecafluoropentylthio, 6-fluorohexylthio, 6-chlorohexylthio, 6-bromohexylthio, 6-iodohexylthio or dodecafluorohexylthio;

C₁-C₄-alkylsulfinyl (C₁-C₄-alkyl-S(═O)—): for example methylsulfinyl, ethylsulfinyl, propylsulfinyl, 1-methylethylsulfinyl, butylsulfinyl, 1-methylpropylsulfinyl, 2-methylpropylsulfinyl or 1,1-dimethylethylsulfinyl;

C₁-C₆-alkylsulfinyl and the alkylsulfinyl radicals of C₁-C₆-alkylsulfinyl-C₁-C₆-alkyl: C₁-C₄-alkylsulfinyl, as mentioned above, and also, for example, pentylsulfinyl, 1-methylbutylsulfinyl, 2-methylbutylsulfinyl, 3-methylbutylsulfinyl, 2,2-dimethylpropylsulfinyl, 1-ethylpropylsulfinyl, 1,1-dimethylpropylsulfinyl, 1,2-dimethylpropylsulfinyl, hexylsulfinyl, 1-methylpentylsulfinyl, 2-methylpentylsulfinyl, 3-methylpentylsulfinyl, 4-methylpentylsulfinyl, 1,1-dimethylbutylsulfinyl, 1,2-dimethylbutylsulfinyl, 1,3-dimethylbutylsulfinyl, 2,2-dimethylbutylsulfinyl, 2,3-dimethylbutylsulfinyl, 3,3-dimethylbutylsulfinyl, 1-ethylbutylsulfinyl, 2-ethylbutylsulfinyl, 1,1,2-trimethylpropylsulfinyl, 1,2,2-trimethyl propylsulfinyl, 1-ethyl-1-methylpropylsulfinyl or 1-ethyl-2-methylpropylsulfinyl;

C₁-C₆-haloalkylsulfinyl: a C₁-C₆-alkylsulfinyl radical as mentioned above which is partially or fully substituted by fluorine, chlorine, bromine and/or iodine, i.e., for example, fluoromethylsulfinyl, difluoromethylsulfinyl, trifluoromethylsulfinyl, chlorodifluoromethylsulfinyl, bromodifluoromethylsulfinyl, 2-fluoroethylsulfinyl, 2-chloroethylsulfinyl, 2-bromoethylsulfinyl, 2-iodoethylsulfinyl, 2,2-difluoroethylsulfinyl, 2,2,2-trifluoroethylsulfinyl, 2,2,2-trichloroethylsulfinyl, 2-chloro-2-fluoroethylsulfinyl, 2-chloro-2,2-difluoroethylsulfinyl, 2,2-dichloro-2-fluoroethylsulfinyl, pentafluoroethylsulfinyl, 2-fluoropropylsulfinyl, 3-fluoropropylsulfinyl, 2-chloropropylsulfinyl, 3-chloropropylsulfinyl, 2-bromopropylsulfinyl, 3-bromopropylsulfinyl, 2,2-difluoropropylsulfinyl, 2,3-difluoropropylsulfinyl, 2,3-dichloropropylsulfinyl, 3,3,3-trifluoropropylsulfinyl, 3,3,3-trichloropropylsulfinyl, 2,2,3,3,3-pentafluoropropylsulfinyl, heptafluoropropylsulfinyl, 1-(fluoromethyl)-2-fluoroethylsulfinyl, 1-(chloromethyl)-2-chloroethylsulfinyl, 1-(bromomethyl)-2-bromoethylsulfinyl, 4-fluorobutylsulfinyl, 4-chlorobutylsulfinyl, 4-bromobutylsulfinyl, nonafluorobutylsulfinyl, 5-fluoropentylsulfinyl, 5-chloropentylsulfinyl, 5-bromopentylsulfinyl, 5-iodopentylsulfinyl, undecafluoropentylsulfinyl, 6-fluorohexylsulfinyl, 6-chaorohexylsulfinyl, 6-bromohexylsulfinyl, 6-iodohexylsulfinyl or dodecafluorohexylsulfinyl;

C₁-C₄-alkylsulfonyl (C₁-C₄-alkyl-S(═O)₂—): for example methylsulfonyl, ethylsulfonyl, propylsulfonyl, 1-methylethylsulfonyl, butylsulfonyl, 1-methylpropylsulfonyl, 2-methylpropyl sulfonyl or 1,1-dimethylethylsulfonyl;

C₁-C₆-alkylsulfonyl, and the alkylsulfonyl radicals of C₁-C₆-alkylsulfonyl-C₃-C₆-alkyl, C₁-C₆-alkylsulfonylamino and N—(C₄-C₆-alkyl)-N—(C₁-C₆-alkylsulfonyl)amino: C₁-C₄-alkylsulfonyl as mentioned above, and also pentylsulfonyl, 1-methylbutylsulfonyl, 2-methylbutylsulfonyl, 3-methylbutylsulfonyl, 1,1-dimethylpropylsulfonyl, 1,2-dimethylpropylsulfonyl, 2,2-dimethylpropylsulfonyl, 1-ethylpropylsulfonyl, hexylsulfonyl, 1-methylpentylsulfonyl, 2-methylpentylsulfonyl, 3-methylpentylsulfonyl, 4-methylpentylsulfonyl, 1,1-dimethylbutylsulfonyl, 1,2-dimethylbutylsulfonyl, 1,3-dimethylbutylsulfonyl, 2,2-dimethylbutylsulfonyl, 2,3-dimethylbutylsulfonyl, 3,3-dimethylbutylsulfonyl, 1-ethylbutylsulfonyl, 2-ethylbutylsulfonyl, 1,1,2-trimethylpropylsulfonyl, 1,2,2-trimethylpropylsulfonyl, 1-ethyl-1-methylpropylsulfonyl or 1-ethyl-2-methylpropylsulfonyl;

C₁-C₆-haloalkylsulfonyl, and the haloalkylsulfonyl radicals of N—(C₁-C₆-haloalkylsulfonyl)amino and N—(C₁-C₆-alkyl)-N—(C₁-C₆-haloalkylsulfonyl)amino: a C₁-₆-alkylsulfonyl radical as mentioned above which is partially or fully substituted by fluorine, chlorine, bromine and/or iodine, i.e., for example, fluoromethylsulfonyl, difluoromethylsulfonyl, trifluoromethylsulfonyl, chlorodifluoromethylsulfonyl, bromodifluoromethylsulfonyl, 2-fluoroethylsulfonyl, 2-chloroethylsulfonyl, 2-bromoethylsulfonyl, 2-iodoethylsulfonyl, 2,2-difluoroethylsulfonyl, 2,2,2-trifluoroethylsulfonyl, 2-chloro-2-fluoroethylsulfonyl, 2-chloro-2,2-difluoroethylsulfonyl, 2,2-dichloro-2-fluoroethylsulfonyl, 2,2,2-trichloroethylsulfonyl, pentafluoroethylsulfonyl, 2-fluoropropylsulfonyl, 3-fluoropropylsulfonyl, 2-chloropropylsulfonyl, 3-chloropropylsulfonyl, 2-bromopropylsulfonyl, 3-bromopropylsulfonyl, 2,2-difluoropropylsulfonyl, 2,3-difluoropropylsulfonyl, 2,3-dichloropropylsulfonyl, 3,3,3-trifluoropropylsulfonyl, 3,3,3-trichloropropylsulfonyl, 2,2,3,3,3-pentafluoropropylsulfonyl, heptafluoropropylsulfonyl, 1-(fluoromethyl)-2-fluoroethylsulfonyl, 1-(chloromethyl)-2-chloroethylsulfonyl, 1-(bromomethyl)-2-bromoethylsulfonyl, 4-fluorobutylsulfonyl, 4-chlorobutylsulfonyl, 4-bromobutylsulfonyl, nonafluorobutylsulfonyl, 5-fluoropentylsulfonyl, 5-chloropentylsulfonyl, 5-bromopentylsulfonyl, 5-iodopentylsulfonyl, 6-fluorohexylsulfonyl, 6-bromohexylsulfonyl, 6-iodohexylsulfonyl or dodecafluorohexylsulfonyl;

C₁-C₆-alkylamino, and the alkylamino radicals of (C₁-C₆-alkoxy)(C₁-C₆-alkyl)amino: for example methylamino, ethylamino, propylamino, 1-methylethylamino, butylamino, 1-methylpropylamino, 2-methylpropylamino, 1,1-dimethylethylamino, pentylamino, 1-methylbutylamino, 2-methylbutylamino, 3-methylbutylamino, 2,2-dimethylpropylamino, 1-ethylpropylamino, hexylamino, 1,1-dimethylpropylamino, 1,2-dimethylpropylamino, 1-methylpentylamino, 2-methylpentylamino, 3-methylpentylamino, 4-methylpentylamino, 1,1-dimethylbutylamino, 1,2-dimethylbutylamino, 1,3-dimethylbutylamino, 2,2-dimethylbutylamino, 2,3-dimethylbutylamino, 3,3-dimethylbutylamino, 1-ethylbutylamino, 2-ethylbutylamino, 1,1,2-trimethylpropylamino, 1,2,2-trimethylpropylamino, 1-ethyl-1-methylpropylamino or 1-ethyl-2-methylpropylamino;

(C₁-C₆-alkylamino)sulfonyl: for example methylaminosulfonyl, ethylaminosulfonyl, propylaminosulfonyl, 1-methylethylaminosulfonyl, butylaminosulfonyl, 1-methylpropylaminosulfonyl, 2-methylpropylaminosulfonyl, 1,1-dimethylethylaminosulfonyl, pentylaminosulfonyl, 1-methylbutylaminosulfonyl, 2-methylbutylaminosulfonyl, 3-methylbutylaminosulfonyl, 2,2-dimethylpropylaminosulfonyl, 1-ethylpropylaminosulfonyl, hexylaminosulfonyl, 1,1-dimethylpropylaminosulfonyl, 1,2-dimethylpropylaminosulfonyl, 1-methylpentylaminosulfonyl, 2-methylpentylaminosulfonyl, 3-methylpentylaminosulfonyl, 4-methylpentylaminosulfonyl, 1,1-dimethylbutylaminosulfonyl, 1,2-dimethylbutylaminosulfonyl, 1,3-dimethylbutylaminosulfonyl, 2,2-dimethylbutylaminosulfonyl, 2,3-dimethylbutylaminosulfonyl, 3,3-dimethylbutylaminosulfonyl, 1-ethylbutylaminosulfonyl, 2-ethylbutylaminosulfonyl, 1,1,2-trimethylpropylaminosulfonyl, 1,2,2-trimethylpropylaminosulfonyl, 1-ethyl-1-methylpropylaminosulfonyl or 1-ethyl-2-methylpropylaminosulfonyl;

di(C₁-C₆-alkyl)aminosulfonyl: for example N,N-dimethylaminosulfonyl, N,N-diethylaminosulfonyl, N,N-di(1-methylethyl)aminosulfonyl, N,N-dipropylaminosulfonyl, N,N-dibutylaminosulfonyl, N,N-di(1-methylpropyl)aminosulfonyl, N,N-di(2-methylpropyl)aminosulfonyl, N,N-di(1,1-dimethylethyl)aminosulfonyl, N-ethyl-N-methylaminosulfonyl, N-methyl-N-propylaminosulfonyl, N-methyl-N-(1-methylethyl)aminosulfonyl, N-butyl-N-methylaminosulfonyl, N-methyl-N-(1-methylpropyl)aminosulfonyl, N-methyl-N-(2-methylpropyl)aminosulfonyl, N-(1,1-dimethylethyl)-N-methylaminosulfonyl, N-ethyl-N-propylaminosulfonyl, N-ethyl-N-(1-methylethyl)aminosulfonyl, N-butyl-N-ethylaminosulfonyl, N-ethyl-N-(1-methylpropyl)aminosulfonyl, N-ethyl-N-(2-methylpropyl)aminosulfonyl, N-ethyl-N-(1,1-dimethylethyl)aminosulfonyl, N-(1-methylethyl)-N-propylaminosulfonyl, N-butyl-N-propylaminosulfonyl, N-(1-methylpropyl)-N-propylaminosulfonyl, N-(2-methylpropyl)-N-propylaminosulfonyl, N-(1,1-dimethylethyl)-N-propylaminosulfonyl, N-butyl-N-(1-methylethyl)aminosulfonyl, N-(1-methylethyl)-N-(1-methylpropyl)aminosulfonyl, N-(1-methylethyl)-N-(2-methylpropyl)aminosulfonyl, N-(1,1-dimethylethyl)-N-(1-methylethyl)aminosulfonyl, N-butyl-N-(1-methylpropyl)aminosulfonyl, N-butyl-N-(2-methylpropyl)aminosulfonyl, N-butyl-N-(1,1-dimethylethyl)aminosulfonyl, N-(1-methylpropyl)-N-(2-methylpropyl)aminosulfonyl, N-(1,1-dimethylethyl)-N-(1-methylpropyl)aminosulfonyl, N-(1,1-dimethylethyl)-N-(2-methylpropyl)aminosulfonyl, N-methyl-N-pentylaminosulfonyl, N-methyl-N-(1-methylbutyl)aminosulfonyl, N-methyl-N-(2-methylbutyl)aminosulfonyl, N-methyl-N-(3-methylbutyl)aminosulfonyl, N-methyl-N-(2,2-dimethylpropyl)aminosulfonyl, N-methyl-N-(1-ethylpropyl)aminosulfonyl, N-methyl-N-hexylaminosulfonyl, N-methyl-N-(1,1-dimethylpropyl)aminosulfonyl, N-methyl-N-(1,2-dimethylpropyl)aminosulfonyl, N-methyl-N-(1-methylpentyl)aminosulfonyl, N-methyl-N-(2-methylpentyl)aminosulfonyl, N-methyl-N-(3-methylpentyl)aminosulfonyl, N-methyl-N-(4-methylpentyl)aminosulfonyl, N-methyl-N-(1,1-dimethylbutyl)aminosulfonyl, N-methyl-N-(1,2-dimethylbutyl)aminosulfonyl, N-methyl-N-(1,3-dimethylbutyl)aminosulfonyl, N-methyl-N-(2,2-dimethylbutyl)aminosulfonyl, N-methyl-N-(2,3-dimethylbutyl)aminosulfonyl, N-methyl-N-(3,3-dimethylbutyl)aminosulfonyl, N-methyl-N-(1-ethylbutyl)aminosulfonyl, N-methyl-N-(2-ethylbutyl)aminosulfonyl, N-methyl-N-(1,1,2-trimethylpropyl)aminosulfonyl, N-methyl-N-(1,2,2-trimethylpropyl)aminosulfonyl, N-methyl-N-(1-ethyl-1-methylpropyl)aminosulfonyl, N-methyl-N-(1-ethyl-2-methylpropyl)aminosulfonyl, N-ethyl-N-pentylaminosulfonyl, N-ethyl-N-(1-methylbutyl)aminosulfonyl, N-ethyl-N-(2-methylbutyl)aminosulfonyl, N-ethyl-N-(3-methylbutyl)aminosulfonyl, N-ethyl-N-(2,2-dimethylpropyl)aminosulfonyl, N-ethyl-N-(1-ethylpropyl)aminosulfonyl, N-ethyl-N-hexylaminosulfonyl, N-ethyl-N-(1,1-dimethylpropyl)aminosulfonyl, N-ethyl-N-(1,2-dimethylpropyl)aminosulfonyl, N-ethyl-N-(1-methylpentyl )aminosulfonyl, N-ethyl-N-(2-methylpentyl)aminosulfonyl, N-ethyl-N-(3-methylpentyl)aminosulfonyl, N-ethyl-N-(4-methylpentyl)aminosulfonyl, N-ethyl-N-(1,1-dimethyl butyl)aminosulfonyl, N-ethyl-N-(1,2-dimethylbutyl)aminosulfonyl, N-ethyl-N-(1,3-dimethylbutyl)aminosulfonyl, N-ethyl-N-(2,2-dimethylbutyl)aminosulfonyl, N-ethyl-N-(2,3-dimethylbutyl)aminosulfonyl, N-ethyl-N-(3,3-dimethylbutyl)aminosulfonyl, N-ethyl-N-(1-ethylbutyl)aminosulfonyl, N-ethyl-N-(2-ethylbutyl)aminosulfonyl, N-ethyl-N-(1,1,2-trimethylpropyl)aminosulfonyl, N-ethyl-N-(1,2,2-trimethylpropyl)aminosulfonyl, N-ethyl-N-(1-ethyl-1-methylpropyl)aminosulfonyl, N-ethyl-N-(1-ethyl-2-methylpropyl)aminosulfonyl, N-propyl-N-pentylaminosulfonyl, N-butyl-N-pentylaminosulfonyl, N,N-dipentylaminosulfonyl, N-propyl-N-hexylaminosulfonyl, N-butyl-N-hexylaminosulfonyl, N-pentyl-N-hexylaminosulfonyl or N,N-dihexylaminosulfonyl;

di(C₁-C₄-alkyl)amino, and the dialkylamino radicals of di(C₁-C₄-alkyl)amino-C₁-C₄-alkoxycarbonyl: for example N,N-dimethylamino, N,N-diethylamino, N,N-dipropylamino, N,N-di(1-methylethyl)amino, N,N-dibutylamino, N,N-di(1-methylpropyl)amino, N,N-di(2-methylpropyl)amino, N,N-di(1,1-dimethylethyl)amino, N-ethyl-N-methylamino, N-methyl-N-propylamino, N-methyl-N-(1-methylethyl)amino, N-butyl-N-methylamino, N-methyl-N-(1-methylpropyl)amino, N-methyl-N-(2-methylpropyl)amino, N-(1,1-dimethylethyl)-N-methylamino, N-ethyl-N-propylamino, N-ethyl-N-(1-methylethyl)amino, N-butyl-N-ethylamino, N-ethyl-N-(1-methylpropyl)amino, N-ethyl-N-(2-methylpropyl)amino, N-ethyl-N-(1,1-dimethylethyl)amino, N-(1-methylethyl)-N-propylamino, N-butyl-N-propylamino, N-(1-methylpropyl)-N-propylamino, N-(2-methylpropyl)-N-propylamino, N-(1,1-dimethylethyl)-N-propylamino, N-butyl-N-(1-methylethyl)amino, N-(1-methylethyl)-N-(1-methylpropyl)amino, N-(1-methylethyl)-N-(2-methylpropyl)amino, N-(1,1-dimethylethyl)-N-(1-methylethyl)amino, N-butyl-N-(1-methylpropyl)amino, N-butyl-N-(2-methylpropyl)amino, N-butyl-N-(1,1-dimethylethyl)amino, N-(1-methylpropyl)-N-(2-methylpropyl)amino, N-(1,1-dimethylethyl)-N-(1-methylpropyl)amino or N-(1,1-dimethylethyl)-N-(2-methylpropyl)amino;

di(C₁-C₆-alkyl)amino: di(C₁-C₄-alkyl)amino as mentioned above, and also N,N-dipentylamino, N,N-dihexylamino, N-methyl-N-pentylamino, N-ethyl-N-pentylamino, N-methyl-N-hexylamino or N-ethyl-N-hexylamino;

C₁-C₄-alkylcarbonyl: for example methylcarbonyl, ethylcarbonyl, propylcarbonyl, 1-methylethylcarbonyl, butylcarbonyl, 1-methylpropylcarbonyl, 2-methylpropylcarbonyl or 1,1-dimethylethylcarbonyl;

C₁-C₆-alkylcarbonyl, and the alkylcarbonyl radicals of C₁-C₆-alkylcarbonyl-C₁-C₆-alkyl: C₁-C₄-alkylcarbonyl as mentioned above, and also, for example, pentylcarbonyl, 1-methylbutylcarbonyl, 2-methylbutylcarbonyl, 3-methylbutylcarbonyl, 2,2-dimethylpropylcarbonyl, 1-ethylpropylcarbonyl, hexylcarbonyl, 1,1-dimethylpropylcarbonyl, 1,2-dimethylpropylcarbonyl, 1-methylpentylcarbonyl, 2-methylpentylcarbonyl, 3-methylpentylcarbonyl, 4-methylpentylcarbonyl, 1,1-dimethylbutylcarbonyl, 1,2-dimethylbutylcarbonyl, 1,3-dimethylbutylcarbonyl, 2,2-dimethylbutylcarbonyl, 2,3-dimethylbutylcarbonyl, 3,3-dimethylbutylcarbonyl, 1-ethylbutylcarbonyl, 2-ethylbutylcarbonyl, 1,1,2-trimethylpropylcarbonyl, 1,2,2-trimethylpropylcarbonyl, 1-ethyl-1-methylpropylcarbonyl or 1-ethyl-2-methylpropylcarbonyl;

C₁-C₂₀-alkylcarbonyl: C₁-C₆-alkylcarbonyl as mentioned above, and also heptylcarbonyl, octylcarbonyl, pentadecylcarbonyl or heptadecylcarbonyl;

C₁-C₆-haloalkylcarbonyl: a C₁-C₆-alkylcarbonyl radical as mentioned above which is partially or fully substituted by fluorine, chlorine, bromine and/or iodine, i.e., for example, chloroacetyl, dichloroacetyl, trichloroacetyl, fluoroacetyl, difluoroacetyl, trifluoroacetyl, chlorofluoroacetyl, dichlorofluoroacetyl, chlorodifluoroacetyl, 2-fluoroethylcarbonyl, 2-chloroethylcarbonyl, 2-bromoethylcarbonyl, 2-iodoethylcarbonyl, 2,2-difluoroethylcarbonyl, 2,2,2-trifluoroethylcarbonyl, 2-chloro-2-fluoroethylcarbonyl, 2-chloro-2,2-difluoroethylcarbonyl, 2,2-dichloro-2-fluoroethylcarbonyl, 2,2,2-trichloroethylcarbonyl, pentafluoroethylcarbonyl, 2-fluoropropylcarbonyl, 3-fluoropropylcarbonyl, 2,2-difluoropropylcarbonyl, 2,3-difluoropropylcarbonyl, 2-chloropropylcarbonyl, 3-chloropropylcarbonyl, 2,3-dichloropropylcarbonyl, 2-bromopropylcarbonyl, 3-bromopropylcarbonyl, 3,3,3-trifluoropropylcarbonyl, 3,3,3-trichloropropylcarbonyl, 2,2,3,3,3-pentafluoropropylcarbonyl, heptafluoropropylcarbonyl, 1-(fluoromethyl)-2-fluoroethylcarbonyl, 1-(chloromethyl)-2-chloroethylcarbonyl, 1-(bromomethyl)-2-bromoethylcarbonyl, 4-fluorobutylcarbonyl, 4-chlorobutylcarbonyl, 4-bromobutylcarbonyl, nonafluorobutylcarbonyl, 5-fluoropentylcarbonyl, 5-chloropentylcarbonyl, 5-bromopentylcarbonyl, perfluoropentylcarbonyl, 6-fluorohexylcarbonyl, 6-chlorohexylcarbonyl, 6-bromohexylcarbonyl or perfluorohexylcarbonyl;

C₁-C₄-alkoxycarbonyl, and the alkoxycarbonyl moieties of di(C₁-C₄-alkyl)amino-C₁-C₄-alkoxycarbonyl: for example methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, 1-methylethoxycarbonyl, butoxycarbonyl, 1-methylpropoxycarbonyl, 2-methylpropoxycarbonyl or 1,1-dimethylethoxycarbonyl;

(C₁-C₆-alkoxy)carbonyl, and the alkoxycarbonyl moieties of C₁-C₆-alkoxycarbonyloxy: (C₁-C₄-alkoxy)carbonyl as mentioned above, and also, for example, pentoxycarbonyl, 1-methylbutoxycarbonyl, 2-methylbutoxycarbonyl, 3-methylbutoxycarbonyl, 2,2-dimethylpropoxycarbonyl, 1-ethylpropoxycarbonyl, hexoxycarbonyl, 1,1-dimethylpropoxycarbonyl, 1,2-dimethylpropoxycarbonyl, 1-methylpentoxycarbonyl, 2-methylpentoxycarbonyl, 3-methylpentoxycarbonyl, 4-methylpentoxycarbonyl, 1,1-dimethylbutoxycarbonyl, 1,2-dimethylbutoxycarbonyl, 1,3-dimethylbutoxycarbonyl, 2,2-dimethylbutoxycarbonyl, 2,3-dimethylbutoxycarbonyl, 3,3-dimethylbutoxycarbonyl, 1-ethylbutoxycarbonyl, 2-ethylbutoxycarbonyl, 1,1,2-trimethylpropoxycarbonyl, 1,2,2-trimethylpropoxycarbonyl, 1-ethyl-1-methylpropoxycarbonyl or 1-ethyl-2-methylpropoxycarbonyl;

C₁-C₆-haloalkoxycarbonyl: a C₁-C₆-alkoxycarbonyl radical as mentioned above which is partially or fully substituted by fluorine, chlorine, bromine and/or iodine, i.e., for example, fluoromethoxycarbonyl, difluoromethoxycarbonyl, trifluoromethoxycarbonyl, chlorodifluoromethoxycarbonyl, bromodifluoromethoxycarbonyl, 2-fluoroethoxycarbonyl, 2-chloroethoxycarbonyl, 2-bromoethoxycarbonyl, 2-iodoethoxycarbonyl, 2,2-difluoroethoxycarbonyl, 2,2,2-trifluoroethoxycarbonyl, 2-chloro-2-fluoroethoxycarbonyl, 2-chloro-2,2-difluoroethoxycarbonyl, 2,2-dichloro-2-fluoroethoxycarbonyl, 2,2,2-trichloroethoxycarbonyl, pentafluoroethoxycarbonyl, 2-fluoropropoxycarbonyl, 3-fluoropropoxycarbonyl, 2-chloropropoxycarbonyl, 3-chloropropoxycarbonyl, 2-bromopropoxycarbonyl, 3-bromopropoxycarbonyl, 2,2-difluoropropoxycarbonyl, 2,3-difluoropropoxycarbonyl, 2,3-dichloropropoxycarbonyl, 3,3,3-trifluoropropoxycarbonyl, 3,3,3-trichloropropoxycarbonyl, 2,2,3,3,3-pentafluoropropoxycarbonyl, heptafluoropropoxycarbonyl, 1-(2fluoromethyl)-2-fluoroethoxycarbonyl, 1-(chloromethyl)-2-chloroethoxycarbonyl, 1-(bromomethyl)-2-bromoethoxycarbonyl, 4-fluorobutoxycarbonyl, 4-chlorobutoxycarbonyl, 4-bromobutoxycarbonyl, 4-iodobutoxycarbonyl, 5-fluoropentoxycarbonyl, 5-chloropentoxycarbonyl, 5-bromopentoxycarbonyl, 6-fluorohexoxycarbonyl, 6-chlorohexoxycarbonyl or 6-bromohexoxycarbonyl;

(C₁-C₄-alkylamino)carbonyl: for example methylaminocarbonyl, ethylaminocarbonyl, propylaminocarbonyl, 1-methylethylaminocarbonyl, butylaminocarbonyl, 1-methylpropylaminocarbonyl, 2-methylpropylaminocarbonyl or 1,1-dimethylethylaminocarbonyl;

(C₁-C₆-alkylamino)carbonyl: (C₁-C₄-alkylamino)carbonyl as mentioned above, and also, for example, pentylaminocarbonyl, 1-methylbutylaminocarbonyl, 2-methylbutylaminocarbonyl, 3-methylbutylaminocarbonyl, 2,2-dimethylpropylaminocarbonyl, 1-ethylpropylaminocarbonyl, hexylaminocarbonyl, 1,1-dimethylpropylaminocarbonyl, 1,2-dimethylpropylaminocarbonyl, 1-methylpentylaminocarbonyl, 2-methylpentylaminocarbonyl, 3-methylpentylaminocarbonyl, 4-methylpentylaminocarbonyl, 1,1-dimethylbutylaminocarbonyl, 1,2-dimethylbutylaminocarbonyl, 1,3-dimethylbutylaminocarbonyl, 2,2-dimethylbutylaminocarbonyl, 2,3-dimethylbutylaminocarbonyl, 3,3-dimethylbutylaminocarbonyl, 1-ethylbutylaminocarbonyl, 2-ethylbutylaminocarbonyl, 1,1,2-trimethylpropylaminocarbonyl, 1,2,2-trimethylpropylaminocarbonyl, 1-ethyl-1-methylpropylaminocarbonyl or 1-ethyl-2-methylpropylaminocarbonyl;

di(C₁-C₄-alkyl)aminocarbonyl: for example N,N-dimethylaminocarbonyl, N,N-diethylaminocarbonyl, N,N-di(1-methylethyl)aminocarbonyl, N,N-dipropylaminocarbonyl, N,N-dibutylaminocarbonyl, N,N-di(1-methylpropyl)aminocarbonyl, N,N-di(2-methylpropyl)aminocarbonyl, N,N-di(1,1-dimethylethyl)aminocarbonyl, N-ethyl-N-methylaminocarbonyl, N-methyl-N-propylaminocarbonyl, N-methyl-N-(1-methylethyl)aminocarbonyl, N-butyl-N-methylaminocarbonyl, N-methyl-N-(1-methylpropyl)aminocarbonyl, N-methyl-N-(2-methylpropyl)aminocarbonyl, N-(1,1-dimethylethyl)-N-methylaminocarbonyl, N-ethyl-N-propylaminocarbonyl, N-ethyl-N-(1-methylethyl)aminocarbonyl, N-butyl-N-ethylaminocarbonyl, N-ethyl-N-(1-methylpropyl)aminocarbonyl, N-ethyl-N-(2-methylpropyl)aminocarbonyl, N-ethyl-N-(1,1-dimethylethyl)aminocarbonyl, N-(1-methylethyl)-N-propylaminocarbonyl, N-butyl-N-propylaminocarbonyl, N-(1-methylpropyl)-N-propylaminocarbonyl, N-(2-methylpropyl)-N-propylaminocarbonyl, N-(1,1-dimethylethyl)-N-propylaminocarbonyl, N-butyl-N-(1-methylethyl)aminocarbonyl, N-(-methylethyl)-N-(1-methylpropyl)aminocarbonyl, N-(1-methylethyl)-N-(2-methylpropyl)aminocarbonyl, N-(1,1-dimethylethyl)-N-(2-methylethyl)aminocarbonyl, N-butyl-N-(1-methylpropyl)aminocarbonyl, N-butyl-N-(2-methylpropyl)aminocarbonyl, N-butyl-N-(1,1-dimethylethyl)aminocarbonyl, N-(1-methylpropyl)-N-(2-methylpropyl)aminocarbonyl, N-(1,1-dimethylethyl)-N-(1-methylpropyl)aminocarbonyl or N-(1,1-dimethylethyl)-N-(2-methylpropyl)aminocarbonyl;

C₁-C₆-alkoxy-C₁-C₆-alkyl: C₁-C₆-alkyl which is substituted by C₁-C₆-alkoxy as mentioned above, i.e., for example, methoxymethyl, ethoxymethyl, propoxymethyl, (1-methylethoxy)methyl, butoxymethyl, (1-methylpropoxy)methyl, (2-methylpropoxy)methyl, (1,1-dimethylethoxy)methyl, 2-(methoxy)ethyl, 2-(ethoxy)ethyl, 2-(propoxy)ethyl, 2-(1-methylethoxy)ethyl, 2-(butoxy)ethyl, 2-(1-methylpropoxy)ethyl, 2-(2-methylpropoxy)ethyl, 2-(1,1-dimethylethoxy)ethyl, 2-(methoxy)propyl, 2-(ethoxy)propyl, 2-(propoxy)propyl, 2-(1-methylethoxy)propyl, 2-(butoxy)propyl, 2-(1-methylpropoxy)propyl, 2-(2-methylpropoxy)propyl, 2-(1,1-dimethylethoxy)propyl, 3-(methoxy)propyl, 3-(ethoxy)propyl, 3-(propoxy)propyl, 3-(1-methylethoxy)propyl, 3-(butoxy)propyl, 3-(1-methylpropoxy)propyl, 3-(2-methylpropoxy)propyl, 3-(1,1-dimethylethoxy)propyl, 2-(methoxy)butyl, 2-(ethoxy)butyl, 2-(propoxy)butyl, 2-(1-methylethoxy)butyl, 2-(butoxy)butyl, 2-(1-methylpropoxy)butyl, 2-(2-methylpropoxy)butyl, 2-(1,1-dimethylethoxy)butyl, 3-(methoxy)butyl, 3-(ethoxy)butyl, 3-(propoxy)butyl, 3-(1-methylethoxy)butyl, 3-(butoxy)butyl, 3-(1-methylpropoxy)butyl, 3-(2-methylpropoxy)butyl, 3-(1,1-dimethylethoxy)butyl, 4-(methoxy)butyl, 4-(ethoxy)butyl, 4-(propoxy)butyl, 4-(1-methylethoxy)butyl, 4-(butoxy)butyl, 4-(1-methylpropoxy)butyl, 4-(2-methylpropoxy)butyl, 4-(1,1-dimethylethoxy)butyl, 5-methoxypentyl, 5-ethoxypentyl, 6-methoxyhexyl or 6-ethoxyhexyl;

the C₁-C₄-alkoxy-C₁-C₄-alkoxy radical of C₁-C₄-alkoxy-C₁-C₄-alkoxycarbonyl: C₁-C₄-alkoxy which is substituted by C₁-C₄-alkoxy as mentioned above, i.e., for example, methoxymethoxy, ethoxymethoxy, propoxymethoxy, (1-methylethoxy)methoxy, butoxymethoxy, (1-methylpropoxy)methoxy, (2-methylpropoxy)methoxy, (1,1-dimethylethoxy)methoxy, 2-(methoxy)ethoxy, 2-(ethoxy)ethoxy, 2-(propoxy)ethoxy, 2-(1-methylethoxy)ethoxy, 2-(butoxy)ethoxy, 2-(1-methylpropoxy)ethoxy, 2-(2-methylpropoxy)ethoxy, 2-(1,1-dimethylethoxy)ethoxy, 2-(methoxy)propoxy, 2-(ethoxy)propoxy, 2-(propoxy)propoxy, 2-(1-methylethoxy)propoxy, 2-(butoxy)propoxy, 2-(1-methylpropoxy)propoxy, 2-(2-methylpropoxy)propoxy, 2-(1,1-dimethylethoxy)propoxy, 3-(methoxy)propoxy, 3-(ethoxy)propoxy, 3-(propoxy)propoxy, 3-(1-methylethoxy)propoxy, 3-(butoxy)propoxy, 3-(1-methylpropoxy)propoxy, 3-(2-methylpropoxy)propoxy, 3-(1,1-dimethylethoxy)propoxy, 2-(methoxy)butoxy, 2-(ethoxy)butoxy, 2-(propoxy)butoxy, 2-(1-methylethoxy)butoxy, 2-(butoxy)butoxy, 2-(1-methylpropoxy)butoxy, 2-(2-methylpropoxy)butoxy, 2-(1,1-dimethylethoxy)butoxy, 3-(methoxy)butoxy, 3-(ethoxy)butoxy, 3-(propoxy)butoxy, 3-(1-methylethoxy)butoxy, 3-(butoxy)butoxy, 3-(1-methylpropoxy)butoxy, 3-(2-methylpropoxy)butoxy, 3-(1,1-dimethylethoxy)butoxy, 4-(methoxy)butoxy, 4-(ethoxy)-butoxy, 4-(propoxy)butoxy, 4-(1-methylethoxy)butoxy, 4-(butoxy)butoxy, 4-(1-methylpropoxy)butoxy, 4-(2-methylpropoxy)butoxy or 4-(1,1-dimethylethoxy)butoxy;

C₃-C₆-alkenyl, and the alkenyl moieties of C₃-C₆-alkenylcarbonyl, C₃-C₆-alkenyloxy, C₃-C₆-alkenylthio, N—(C₃-C₆-alkenyl)-N—(C₁-C₆-alkyl)amino and di(C₃-C₆-alkenyl)amino: for example prop-2-en-1-yl, but-1-en-4-yl, 1-methylprop-2-en-1-yl, 2-methylprop-2-en-1-yl, 2-buten-1-yl, 1-penten-3-yl, 1-penten-4-yl, 2-penten-4-yl, 1-methylbut-2-en-1-yl, 2-methylbut-2-en-1-yl, 3-methylbut-2-en-1-yl, 1-methylbut-3-en-1-yl, 2-methylbut-3-en-1-yl, 3-methylbut-3-en-1-yl, 1,1-dimethylprop-2-en-1-yl, 1,2-dimethylprop-2-en-1-yl, 1-ethylprop-2-en-1-yl, hex-3-en-1-yl, hex-4-en-1-yl, hex-5-en-1-yl, 1-methylpent-3-en-1-yl, 2-methylpent-3-en-1-yl, 3-methylpent-3-en-1-yl, 4-methylpent-3-en-1-yl, 1-methylpent-4-en-1-yl, 2-methylpent-4-en-1-yl, 3-methylpent-4-en-1-yl, 4-methylpent-4-en-1-yl, 1,1-dimethylbut-2-en-1-yl, 1,1-dimethylbut-3-en-1-yl, 1,2-dimethylbut-2-en-1-yl, 1,2-dimethylbut-3-en-1-yl, 1,3-dimethylbut-2-en-1-yl, 1,3-dimethylbut-3-en-1-yl, 2,2-dimethylbut-3-en-1-yl, 2,3-dimethylbut-2-en-1-yl, 2,3-dimethylbut-3-en-1-yl, 3,3-dimethylbut-2-en-1-yl, 1-ethylbut-2-en-1-yl, 1-ethylbut-3-en-1-yl, 2-ethylbut-2-en-1-yl, 2-ethylbut-3-en-1-yl, 1,1,2-trimethylprop-2-en-1-yl, 1-ethyl-1-methylprop-2-en-1-yl or 1-ethyl-2-methylprop-2-en-1-yl;

C₂-C₆-alkenyl, and the alkenyl moieties of C₂-C₆-alkenylcarbonyl: C₃-C₆-alkenyl as mentioned above, and also ethenyl;

C₃-C₆-haloalkenyl: a C₃-C₆-alkenyl radical as mentioned above which is partially or fully substituted by fluorine, chlorine, bromine and/or iodine, i.e., for example, 2-chloroallyl, 3-chloroallyl, 2,3-dichloroallyl, 3,3-dichloroallyl, 2,3,3-trichloroallyl, 2,3-dichlorobut-2-enyl, 2-bromoallyl, 3-bromoallyl, 2,3-dibromoallyl, 3,3-dibromoallyl, 2,3,3-tribromoallyl or 2,3-dibromobut-2-enyl;

C₃-C₆-alkynyl, and the alkynyl moieties of C₃-C₆-alkynylcarbonyl, C₃-C₆-alkynyloxy, C₃-C₆-alkynylthio, N—(C₃-C₆-alkynyl)-N—(C₁-C₆-alkyl)amino and di(C₃-C₆-alkynyl)amino: for example propargyl, but-1-yn-3-yl, but-1-yn-4-yl, but-2-yn-1-yl, pent-1-yn-3-yl, pent-1-yn-4-yl, pent-1-yn-5-yl, pent-2-yn-1-yl, pent-2-yn-4-yl, pent-2-yn-5-yl, 3-methylbut-1-yn-3-yl, 3-methylbut-1-yn-4-yl, hex-1-yn-3-yl, hex-1-yn-4-yl, hex-1-yn-5-yl, hex-1-yn-6-yl, hex-2-yn-1-yl, hex-2-yn-4-yl, hex-2-yn-5-yl, hex-2-yn-6-yl, hex-3-yn-1-yl, hex-3-yn-2-yl, 3-methylpent-1-yn-3-yl, 3-methylpent-1-yn-4-yl, 3-methylpent-1-yn-5-yl, 4-methylpent-2-yn-4-yl or 4-methylpent-2-yn-5-yl;

C₂-C₆-alkynyl, and the alkynyl moieties of C₂-C₆-alkynylcarbonyl: C₃-C₆-alkynyl as mentioned above, and also ethynyl;

C₃-C₆-haloalkynyl: a C₃-C₆-alkynyl radical as mentioned above which is partially or fully substituted by fluorine, chlorine, bromine and/or iodine, i.e., for example, 1,1-difluoroprop-2-yn-1-yl, 3-iodoprop-2-yn-1-yl, 4-fluorobut-2-yn-1-yl, 4-chlorobut-2-yn-1-yl, 1,1-difluorobut-2-yn-1-yl, 4-iodobut-3-yn-1-yl, 5-fluoropent-3-yn-1-yl, 5-iodopent-4-yn-1-yl, 6-fluorohex-4-yn-1-yl or 6-iodohex-5-yn-1-yl;

C₃-C₆-cycloalkyl, and the cycloalkyl moieties of C₃-C₆-cycloalkylcarbonyl: for example cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl;

C₃-C₆-halocycloalkyl: a C₃-C₆-cycloalkyl radical as mentioned above which may be partially or fully substituted by fluorine, chlorine, bromine and/or iodine, i.e., for example, 2,2-dichlorocycloprop-1-yl, 2,2-difluorocycloprop-1-yl, 3-chlorocyclopent-1-yl, 3-fluorocyclopent-1-yl, 3-bromocyclopent-1-yl, 3,3-dichlorocyclopent-1-yl, 3,3-difluorocyclopent-1-yl, 4-chlorocyclohex-1-yl, 4-fluorocyclohex-1-yl, 4-bromocyclohex-1-yl, 4,4-dichlorocyclohex-1-yl or 4,4-difluorocyclohex-1-yl;

heterocyclyl, and the heterocyclyl moieties of heterocyclylcarbonyl, heterocyclyl-C₁-C₆-alkyl, heterocyclyloxy, heterocyclylaminocarbonyl: a saturated, partially saturated or unsaturated 5- or 6-membered heterocyclic ring which is attached via carbon and contains one to four identical or different heteroatoms selected from the following group: oxygen, sulfur and nitrogen, i.e., for example, 5-membered rings such as:

tetrahydrofuran-2-yl, tetrahydrofuran-3-yl, tetrahydrothien-2-yl, tetrahydrothien-3-yl, tetrahydropyrrol-2-yl, tetrahydropyrrol-3-yl, 2,3-dihydrofuran-2-yl, 2,3-dihydrofuran-3-yl, 2,5-dihydrofuran-2-yl, 2,5-dihydrofuran-3-yl, 4,5-dihydrofuran-2-yl, 4,5-dihydrofuran-3-yl, 2,3-dihydrothien-2-yl, 2,3-dihydrothien-3-yl, 2,5-dihydrothien-2-yl, 2,5-dihydrothien-3-yl, 4,5-dihydrothien-2-yl, 4,5-dihydrothien-3-yl, 2,3-dihydro-1H-pyrrol-2-yl, 2,3-dihydro-1H-pyrrol-3-yl, 2,5-dihydro-1H-pyrrol-2-yl, 2,5-dihydro-1H-pyrrol-3-yl, 4,5-dihydro-1H-pyrrol-2-yl, 4,5-dihydro-1H-pyrrol-3-yl, 3,4-dihydro-2H-pyrrol-2-yl, 3,4-dihydro-2H-pyrrol-3-yl, 3,4-dihydro-5H-pyrrol-2-yl, 3,4-dihydro-5H-pyrrol-3-yl, 2-furyl, 3-furyl, 2-thienyl, 3-thienyl, pyrrol-2-yl, pyrrol-3-yl, tetrahydropyrazol-3-yl, tetrahydropyrazol-4-yl, tetrahydroisoxazol-3-yl, tetrahydroisoxazol-4-yl, tetrahydroisoxazol-5-yl, 1,2-oxathiolan-3-yl, 1,2-oxathiolan-4-yl, 1,2-oxathiolan-5-yl, tetrahydroisothiazol-3-yl, tetrahydroisothiazol-4-yl, tetrahydroisothiazol-5-yl, 1,2-dithiolan-3-yl, 1,2-dithiolan-4-yl, tetrahydroimidazol-2-yl, tetrahydroimidazol-4-yl, tetrahydrooxazol-2-yl, tetrahydrooxazol-4-yl, tetrahydrooxazol-5-yl, tetrahydrothiazol-2-yl, tetrahydrothiazol-4-yl, tetrahydrothiazol-5-yl, 1,3-dioxolan-2-yl, 1,3-dioxolan-4-yl, 1,3-oxathiolan-2-yl, 1,3-oxathiolan-4-yl, 1,3-oxathiolan-5-yl, 1,3-dithiolan-2-yl, 1,3-dithiolan-4-yl, 4,5-dihydro-1H-pyrazol-3-yl, 4,5-dihydro-1H-pyrazol-4-yl, 4,5-dihydro-1H-pyrazol-5-yl, 2,5-dihydro-1H-pyrazol-3-yl, 2,5-dihydro-1H-pyrazol-4-yl, 2,5-dihydro-1H-pyrazol-5-yl, 4,5-dihydroisoxazol-3-yl, 4,5-dihydroisoxazol-4-yl, 4,5-dihydroisoxazol-5-yl, 2,5-dihydroisoxazol-3-yl, 2,5-dihydroisoxazol-4-yl, 2,5-dihydroisoxazol-5-yl, 2,3-dihydroisoxazol-3-yl, 2,3-dihydroisoxazol-4-yl, 2,3-dihydroisoxazol-5-yl, 4,5-dihydroisothiazol-3-yl, 4,5-dihydroisothiazol-4-yl, 4,5-dihydroisothiazol-5-yl, 2,5-dihydroisothiazol-3-yl, 2,5-dihydroisothiazol-4-yl, 2,5-dihydroisothiazol-5-yl, 2,3-dihydroisothiazol-3-yl, 2,3-dihydroisothiazol-4-yl, 2,3-dihydroisothiazol-5-yl, Δ³-1,2-dithiol-3-yl, Δ³-1,2-dithiol-4-yl, Δ³-1,2-dithiol-5-yl, 4,5-dihydro-1H-imidazol-2-yl, 4,5-dihydro-1H-imidazol-4-yl, 4,5-dihydro-1H-imidazol-5-yl, 2,5-dihydro-1H-imidazol-2-yl, 2,5-dihydro-1H-imidazol-4-yl, 2,5-dihydro-1H-imidazol-5-yl, 2,3-dihydro-1H-imidazol-2-yl, 2,3-dihydro-1H-imidazol-4-yl, 4,5-dihydrooxazol-2-yl, 4,5-dihydrooxazol-4-yl, 4,5-dihydrooxazol-5-yl, 2,5-dihydrooxazol-2-yl, 2,5-dihydrooxazol-4-yl, 2,5-dihydrooxazol-5-yl, 2,3-dihydrooxazol-2-yl, 2,3-dihydrooxazol-4-yl, 2,3-dihydrooxazol-5-yl, 4,5-dihydrothiazol-2-yl, 4,5-dihydrothiazol-4-yl, 4,5-dihydrothiazol-5-yl, 2,5-dihydrothiazol-2-yl, 2,5-dihydrothiazol-4-yl, 2,5-dihydrothiazol-5-yl, 2,3-dihydrothiazol-2-yl, 2,3-dihydrothiazol-4-yl, 2,3-dihydrothiazol-5-yl, 1,3-dioxol-2-yl, 1,3-dioxol-4-yl, 1,3-dithiol-2-yl, 1,3-dithiol-4-yl, 1,3-oxathiol-2-yl, 1,3-oxathiol-4-yl, 1,3-oxathiol-5-yl, pyrazol-3-yl, pyrazol-4-yl, isoxazol-3-yl, isoxazol-4-yl, isoxazol-5-yl, isothiazol-3-yl, isothiazol-4-yl, isothiazol-5-yl, imidazol-2-yl, imidazol-4-yl, oxazol-2-yl, oxazol-4-yl, oxazol-5-yl, thiazol-2-yl, thiazol-4-yl, thiazol-5-yl, 1,2,3-Δ²-oxadiazolin-4-yl, 1,2,3-Δ²-oxadiazolin-5-yl, 1,2,4-Δ⁴-oxadiazolin-3-yl, 1,2,4-Δ⁴-oxadiazolin-5-yl, 1,2,4-Δ²-oxadiazolin-3-yl, 1,2,4-Δ²-oxadiazolin-5-yl, 1,2,4-Δ³-oxadiazolin-3-yl, 1,2,4-Δ³-oxadiazolin-5-yl, 1,3,4-Δ²-oxadiazolin-2-yl, 1,3,4-Δ²-oxadiazolin-5-yl, 1,3,4-Δ³-oxadiazolin-2-yl, 1,3,4-oxadiazolin-2-yl, 1,2,4-Δ⁴-thiadiazolin-3-yl, 1,2,4-Δ⁴-thiadiazolin-5-yl, 1,2,4-Δ³-thiadiazolin-3-yl, 1,2,4-Δ³-thiadiazolin-5-yl, 1,2,4-Δ²-thiadiazolin-3-yl, 1,2,4-Δ²-thiadiazolin-5-yl, 1,3,4-Δ²-thiadiazolin-2-yl, 1,3,4-Δ²-thiadiazolin-5-yl, 1,3,4-Δ³-thiadiazolin-2-yl, 1,3,4-thiadiazolin-2-yl, 1,3,2-dioxathiolan-4-yl, 1,2,3-Δ²-triazolin-4-yl, 1,2,3-Δ²-triazolin-5-yl, 1,2,4-Δ²-triazolin-3-yl, 1,2,4-Δ²-triazolin-5-yl, 1,2,4-Δ³-triazolin-3-yl, 1,2,4-Δ³-triazolin-5-yl, 1,2,4-Δ¹-triazolin-2-yl, 1,2,4-triazolin-3-yl, 3H-1,2,4-dithiazol-5-yl, 2H-1,3,4-dithiazol-5-yl, 2H-1,3,4-oxathiazol-5-yl, 1,2,3-oxadiazol-4-yl, 1,2,3-oxadiazol-5-yl, 1,2,4-oxadiazol-3-yl, 1,2,4,-oxadiazol-5-yl, 1,3,4-oxadiazol-2-yl, 1,2,3-thiadiazol-4-yl, 1,2,3-thiadiazol-5-yl, 1,2,4-thiadiazol-3-yl, 1,2,4-thiadiazol-5-yl, 1,3,4-thiadiazolyl-2-yl, 1,2,3-triazol-4-yl, 1,2,4-triazol-3-yl, tetrazol-5-yl,

6-membered rings such as:

tetrahydropyran-2-yl, tetrahydropyran-3-yl, tetrahydropyran-4-yl, piperidin-2-yl, piperidin-3-yl, piperidin-4-yl, tetrahydrothiopyran-2-yl, tetrahydrothiopyran-3-yl, tetrahydrothiopyran-4-yl, 2H-3,4-dihydropyran-6-yl, 2H-3,4-dihydropyran-5-yl, 2H-3,4-dihydropyran-4-yl, 2H-3,4-dihydropyran-3-yl, 2H-3,4-dihydropyran-2-yl, 2H-3,4-dihydropyran-6-yl, 2H-3,4-dihydrothiopyran-5-yl, 2H-3,4-dihydrothiopyran-4-yl, 2H-3,4-dihydropyran-3-yl, 2H-3,4-dihydropyran-2-yl, 1,2,3,4-tetrahydropyridin-6-yl, 1,2,3,4-tetrahydropyridin-5-yl, 1,2,3,4-tetrahydropyridin-4-yl, 1,2,3,4-tetrahydropyridin-3-yl, 1,2,3,4-tetrahydropyridin-2-yl, 2H-5,6-dihydropyran-2-yl, 2H-5,6-dihydropyran-3-yl, 2H-5,6-dihydropyran-4-yl, 2H-5,6-dihydropyran-5-yl, 2H-5,6-dihydropyran-6-yl, 2H-5,6-dihydrothiopyran-2-yl, 2H-5,6-dihydrothiopyran-3-yl, 2H-5,6-dihydrothiopyran-4-yl, 2H-5,6-dihydrothiopyran-5-yl, 2H-5,6-dihydrothiopyran-6-yl, 1,2,5,6-tetrahydropyridin-2-yl, 1,2,5,6-tetrahydropyridin-3-yl, 1,2,5,6-tetrahydropyridin-4-yl, 1,2,5,6-tetrahydropyridin-5-yl, 1,2,5,6-tetrahydropyridin-6-yl, 2,3,4,5-tetrahydropyridin-2-yl, 2,3,4,5-tetrahydropyridin-3-yl, 2,3,4,5-tetrahydropyridin-4-yl, 2,3,4,5-tetrahydropyridin-5-yl, 2,3,4,5-tetrahydropyridin-6-yl, 4H-pyran-2-yl, 4H-pyran-3-yl, 4H-pyran-4-yl, 4H-thiopyran-2-yl, 4H-thiopyran-3-yl, 4H-thiopyran-4-yl, 1,4-dihydropyridin-2-yl, 1,4-dihydropyridin-3-yl, 1,4-dihydropyridin-4-yl, 2H-pyran-2-yl, 2H-pyran-3-yl, 2H-pyran-4-yl, 2H-pyran-5-yl, 2H-pyran-6-yl, 2H-thiopyran-2-yl, 2H-thiopyran-3-yl, 2H-thiopyran-4-yl, 2H-thiopyran-5-yl, 2H-thiopyran-6-yl, 1,2-dihydropyridin-2-yl, 1,2-dihydropyridin-3-yl, 1,2-dihydropyridin-4-yl, 1,2-dihydropyridin-5-yl, 1,2-dihydropyridin-6-yl, 3,4-dihydropyridin-2-yl, 3,1-dihydropyridin-3-yl, 3,4-dihydropyridin-4-yl, 3,4-dihydropyridin-5-yl, 3,4-dihydropyridin-6-yl, 2,5-dihydropyridin-2-yl, 2,5-dihydropyridin-3-yl, 2,5-dihydropyridin-4-yl, 2,5-dihydropyridin-5-yl, 2,5-dihydropyridin-6-yl, 2,3-dihydropyridin-2-yl, 2,3-dihydropyridin-3-yl, 2,3-dihydropyridin-4-yl, 2,3-dihydropyridin-5-yl, 2,3-dihydropyridin-6-yl, pyridin-2-yl, pyridin-3-yl, pyridin-4-yl, 1,3-dioxan-2-yl, 1,3-dioxan-4-yl, 1,3-dioxan-5-yl, 1,4-dioxan-2-yl, 1,3-dithian-2-yl, 1,3-dithian-4-yl, 1,3-dithian-5-yl, 1,4-dithian-2-yl, 1,3-oxathian-2-yl, 1,3-oxathian-4-yl, 1,3-oxathian-5-yl, 1,3-oxathian-6-yl, 1,4-oxathian-2-yl, 1,4-oxathian-3-yl, 1,2-dithian-3-yl, 1,2-dithian-4-yl, hexahydropyrimidin-2-yl, hexahydropyrimidin-4-yl, hexahydropyrimidin-5-yl, hexahydropyrazin-2-yl, hexahydropyridazin-3-yl, hexahydropyridazin-4-yl, tetrahydro-1,3-oxazin-2-yl, tetrahydro-1,3-oxazin-4-yl, tetrahydro-1,3-oxazin-5-yl, tetrahydro-1,3-oxazin-6-yl, tetrahydro-1,3-thiazin-2-yl, tetrahydro-1,3-thiazin-4-yl, tetrahydro-1,3-thiazin-5-yl, tetrahydro-1,3-thiazin-6-yl, tetrahydro-1,4-thiazin-2-yl, tetrahydro-1,4-thiazin-3-yl, tetrahydro-1,4-oxazin-2-yl, tetrahydro-1,4-oxazin-3-yl, tetrahydro-1,2-oxazin-3-yl, tetrahydro-1,2-oxazin-4-yl, tetrahydro-1,2-oxazin-5-yl, tetrahydro-1,2-oxazin-6-yl, 2H-5,6-dihydro-1,2-oxazin-3-yl, 2H-5,6-dihydro-1,2-oxazin-4-yl, 2H-5,6-dihydro-1,2-oxazin-5-yl, 2H-5,6-dihydro-1,2-oxazin-6-yl, 2H-5,6-dihydro-1,2-thiazin-3-yl, 2H-5,6-dihydro-1,2-thiazin-4-yl, 2H-5,6-dihydro-1,2-thiazin-5-yl, 2H-5,6-dihydro-1,2-thiazin-6-yl, 4H-5,6-dihydro-1,2-oxazin-3-yl, 4H-5,6-dihydro-1,2-oxazin-4-yl, 4H-5,6-dihydro-1,2-oxazin-5-yl, 4H-5,6-dihydro-1,2-oxazin-6-yl, 4H-5,6-dihydro-1,2-thiazin-3-yl, 4H-5,6-dihydro-1,2-thiazin-4-yl, 4H-5,6-dihydro-1,2-thiazin-5-yl, 4H-5,6-dihydro-1,2-thiazin-6-yl, 2H-3,6-dihydro-1,2-oxazin-3-yl, 2H-3,6-dihydro-1,2-oxazin-4-yl, 2H-3,6-dihydro-1,2-oxazin-5-yl, 2H-3,6-dihydro-1,2-oxazin-6-yl, 2H-3,6-dihydro-1,2-thiazin-3-yl, 2H-3,6-dihydro-1,2-thiazin-4-yl, 2H-3,6-dihydro-1,2-thiazin-5-yl, 2H-3,6-dihydro-1,2-thiazin-6-yl, 2H-3,4-dihydro-1,2-oxazin-3-yl, 2H-3,4-dihydro-1,2-oxazin-4-yl, 2H-3,4-dihydro-1,2-oxazin-5-yl, 2H-3,4-dihydro-1,2-oxazin-6-yl, 2H-3,4-dihydro-1,2-thiazin-3-yl, 2H-3,4-dihydro-1,2-thiazin-4-yl, 2H-3,4-dihydro-1,2-thiazin-5-yl, 2H-3,4-dihydro-1,2-thiazin-6-yl, 2,3,4,5-tetrahydropyridazin-3-yl, 2,3,4,5-tetrahydropyridazin-4-yl, 2,3,4,5-tetrahydropyridazin-5-yl, 2,3,4,5-tetrahydropyridazin-6-yl, 3,4,5,6-tetrahydropyridazin-3-yl, 3,4,5,6-tetrahydropyridazin-4-yl, 1,2,5,6-tetrahydropyridazin-3-yl, 1,2,5,6-tetrahydropyridazin-4-yl, 1,2,5,6-tetrahydropyridazin-5-yl, 1,2,5,6-tetrahydropyridazin-6-yl, 1,2,3,6-tetrahydropyridazin-3-yl, 1,2,3,6-tetrahydropyridazin-4-yl, 4H-5,6-dihydro-1,3-oxazin-2-yl, 4H-5,6-dihydro-1,3-oxazin-4-yl, 4H-5,6-dihydro-1,3-oxazin-5-yl, 4H-5,6-dihydro-1,3-oxazin-6-yl, 4H-5,6-dihydro-1,3-thiazin-2-yl, 4H-5,6-dihydro-1,3-thiazin-4-yl, 4H-5,6-dihydro-1,3-thiazin-5-yl, 4H-5,6-dihydro-1,3-thiazin-6-yl, 3,4,5-6-tetrahydropyrimidin-2-yl, 3,4,5,6-tetrahydropyrimidin-4-yl, 3,4,5,6-tetrahydropyrimidin-5-yl, 3,4,5,6-tetrahydropyrimidin-6-yl, 1,2,3,4-tetrahydropyrazin-2-yl, 1,2,3,4-tetrahydropyrazin-5-yl, 1,2,3,4-tetrahydropyrimidin-2-yl, 1,2,3,4-tetrahydropyrimidin-4-yl, 1,2,3,4-tetrahydropyrimidin-5-yl, 1,2,3,4-tetrahydropyrimidin-6-yl, 2,3-dihydro-1,4-thiazin-2-yl, 2,3-dihydro-1,4-thiazin-3-yl, 2,3-dihydro-1,4-thiazin-5-yl, 2,3-dihydro-1,4-thiazin-6-yl, 2H-1,2-oxazin-3-yl, 2H-1,2-oxazin-4-yl, 2H-1,2-oxazin-5-yl, 2H-1,2-oxazin-6-yl, 2H-1,2-thiazin-3-yl, 2H-1,2-thiazin-4-yl, 2H-1,2-thiazin-5-yl, 2H-1,2-thiazin-6-yl, 4H-1,2-oxazin-3-yl, 4H-1,2-oxazin-4-yl, 4H-1,2-oxazin-5-yl, 4H-1,2-oxazin-6-yl, 4H-1,2-thiazin-3-yl, 4H-1,2-thiazin-4-yl, 4H-1,2-thiazin-5-yl, 4H-1,2-thiazin-6-yl, 6H-1,2-oxazin-3-yl, 6H-1,2-oxazin-4-yl, 6H-1,2-oxazin-5-yl, 6H-1,2-oxazin-6-yl, 6H-1,2-thiazin-3-yl, 6H-1,2-thiazin-4-yl, 6H-1,2-thiazin-5-yl, 6H-1,2-thiazin-6-yl, 2H-1,3-oxazin-2-yl, 2H-1,3-oxazin-4-yl, 2H-1,3-oxazin-5-yl, 2H-1,3-oxazin-6-yl, 2H-1,3-thiazin-2-yl, 2H-1,3-thiazin-4-yl, 2H-1,3-thiazin-5-yl, 2H-1,3-thiazin-6-yl, 4H-1,3-oxazin-2-yl, 4H-1,3-oxazin-4-yl, 4H-1,3-oxazin-5-yl, 4H-1,3-oxazin-6-yl, 4H-1,3-thiazin-2-yl, 4H-1,3-thiazin-4-yl, 4H-1,3-thiazin-5-yl, 4H-1,3-thiazin-6-yl, 6H-1,3-oxazin-2-yl, 6H-1,3-oxazin-4-yl, 6H-1,3-oxazin-5-yl, 6H-1,3-oxazin-6-yl, 6H-1,3-thiazin-2-yl, 6H-1,3-oxazin-4-yl, 6H-1,3-oxazin-5-yl, 6H-1,3-thiazin-6-yl, 2H-1,4-oxazin-2-yl, 2H-1,4-oxazin-3-yl, 2H-1,4-oxazin-5-yl, 2H-1,4-oxazin-6-yl, 2H-1,4-thiazin-2-yl, 2H-1,4-thiazin-3-yl, 2H-1,4-thiazin-5-yl, 2H-1,4-thiazin-6-yl, 4H-1,4-oxazin-2-yl, 4H-1,4-oxazin-3-yl, 4H-1,4-thiazin-2-yl, 4H-1,4-thiazin-3-yl, 1,4-dihydropyridazin-3-yl, 1,4-dihydropyridazin-4-yl, 1,4-dihydropyridazin-5-yl, 1,4-dihydropyridazin-6-yl, 1,4-dihydropyrazin-2-yl, 1,2-dihydropyrazin-2-yl, 1,2-dihydropyrazin-3-yl, 1,2-dihydropyrazin-5-yl, 1,2-dihydropyrazin-6-yl, 1,4-dihydropyrimidin-2-yl, 1,4-dihydropyrimidin-4-yl, 1,4-dihydropyrimidin-5-yl, 1,4-dihydropyrimidin-6-yl, 3,4-dihydropyrimidin-2-yl, 3,4-dihydropyrimidin-4-yl, 3,4-dihydropyrimidin-5-yl or 3,4-dihydropyrimidin-6-yl, pyridazin-3-yl, pyridazin-4-yl, pyrimidin-2-yl, pyrimidin-4-yl, pyrimidin-5-yl, pyrazin-2-yl, 1,3,5-triazin-2-yl, 1,2,4-triazin-3-yl, 1,2,4-triazin-5-yl, 1,2,4-triazin-6-yl, 1,2,4,5-tetrazin-3-yl;

where, if appropriate, the sulfur of the abovementioned heterocycles can oxidized to S═O or S(═O)₂;

and where a bicyclic ring system may be formed with a fused-on phenyl ring or a C₃-C₆-carbocycle or with a further 5- to 6-membered heterocycle.

N-bonded heterocyclyl: a saturated, partially saturated or unsaturated 5- or 6-membered heterocyclic ring which is attached via nitrogen and contains at least one nitrogen and, if appropriate, one to three identical or different heteroatoms selected from the following group: oxygen, sulfur or nitrogen, i.e., for example

N-bonded 5-membered rings such as:

tetrahydropyrrol-1-yl, 2,3-dihydro-1H-pyrrol-1-yl, 2,5-dihydro-1H-pyrrol-1-yl, pyrrol-1-yl, tetrahydropyrazol-1-yl, tetrahydroisoxazol-2-yl, tetrahydroisothiazol-2-yl, tetrahydroimidazol-1-yl, tetrahydrooxazol-3-yl, tetrahydrothiazol-3-yl, 4,5-dihydro-1H-pyrazol-1-yl, 2,5-dihydro-1H-pyrazol-1-yl, 2,3-dihydro-1H-pyrazol-1-yl, 2,5-dihydroisoxazol-2-yl, 2,3-dihydroisoxazol-2-yl, 2,5-dihydroisothiazol-2-yl, 2,3-dihydroisoxazol-2-yl, 4,5-dihydro-1H-imidazol-1-yl, 2,5-dihydro-1H-imidazol-1-yl, 2,3-dihydro-1H-imidazol-1-yl, 2,3-dihydrooxazol-3-yl, 2,3-dihydrothiazol-3-yl, pyrazol-1-yl, imidazol-1-yl, 1,2,4-Δ⁴-oxadiazolin-2-yl, 1,2,4-Δ²-oxadiazolin-4-yl, 1,2,4-Δ³-oxadiazolin-2-yl, 1,3,4-Δ²-oxadiazolin-4-yl, 1,2,4-Δ⁵-thiadiazolin-2-yl, 1,2,4-Δ³-thiadiazolin-2-yl, 1,2,4-Δ²-thiadiazolin-4-yl, 1,3,4-Δ²-thiadiazolin-4-yl, 1,2,3-Δ²-triazolin-1-yl, 1,2,4-Δ²-triazolin-1-yl, 1,2,4-Δ²-triazolin-4-yl, 1,2,4-Δ³-triazolin-1-yl, 1,2,4-Δ¹-triazolin-4-yl, 1,2,3-triazol-1-yl, 1,2,4-triazol-1-yl, tetrazol-1-yl;

and N-bonded 6-membered rings such as:

piperidin-1-yl, 1,2,3,4-tetrahydropyridin-1-yl, 1,2,5,6-tetrahydropyridin-1-yl, 1,4-dihydropyridin-1-yl, 1,2-dihydropyridin-1-yl, hexahydropyrimidin-1-yl, hexahydropyrazin-1-yl, hexahydropyridazin-1-yl, tetrahydro-1,3-oxazin-3-yl, tetrahydro-1,3-thiazin-3-yl, tetrahydro-1,4-thiazin-4-yl, tetrahydro-1,4-oxazin-4-yl, tetrahydro-1,2-oxazin-2-yl, 2H-5,6-dihydro-1,2-oxazin-2-yl, 2H-5,6-dihydro-1,2-thiazin-2-yl, 2H-3,6-dihydro-1,2-oxazin-2-yl, 2H-3,6-dihydro-1,2-thiazin-oxazin-2-yl, 2H-3,4-dihydro-1,2-thiazin-2-yl, 2,3,4,5-tetrahydropyridazin-2-yl, 1,2,5,6-tetrahydropyridazin-1-yl, 1,2,5,6-tetrahydropyridazin-2-yl, 1,2, 3,6-tetrahydropyridazin-1-yl, 3,4,5,6-tetrahydropyrimidin-3-yl, 1,2,3,4-tetrahydropyrazin-1-yl, 1,2,3,4-tetrahydropyrimidin-1-yl, 1,2,3,4-tetrahydropyrimidin-3-yl, 2,3-dihydro-1,4-thiazin-4-yl, 2H-1,2-oxazin-2-yl, 2H-1,2-thiazin-2-yl, 4H-1,4-oxazin-4-yl, 4H-1,4-thiazin-4-yl, 1,4-dihydropyridazin-1-yl, 1,4-dihydropyrazin-1-yl, 1,2-dihydropyrazin-1-yl, 1,4-dihydropyrimidin-1-yl or 3,4-dihydropyrimidin-3-yl, and

N-bonded cyclic imides such as:

phthalimide, tetrahydrophthalimide, succinimide, maleimide or glutarimide, and also 4-oxo-1,4-dihydropyridin-1-yl.

All phenyl rings or heterocyclyl radicals and all phenyl components in phenyl-C₁-C₆-alkyl, phenoxy, phenylcarbonyl and phenylaminocarbonyl or heterocyclyl components in heterocyclyl-C₁-C₆-alkyl, heterocyclyloxy, heterocyclylcarbonyl and heterocyclylaminocarbonyl are, unless stated otherwise, preferably unsubstituted or they carry one to three halogen atoms and/or one nitro group, one cyano radical and/or one or two methyl, trifluoromethyl, methoxy or trifluoromethoxy substituents.

Suitable heterocycyl radicals are, in particular, 5-membered aromatic heterocycles, for example 2-furyl, 3-furyl, 2-thienyl, 3-thienyl, pyrrol-2-yl, pyrrol-3-yl, pyrazol-3-yl, pyrazol-4-yl, isoxazol-3-yl, isoxazol-4-yl, isoxazol-5-yl, isothiazol-3-yl, isothiazol-4-yl, isothiazol-5-yl, imidazol-2-yl, imidazol-4-yl, oxazol-2-yl, oxazol-4-yl, oxazol-5-yl, thiazol-2-yl, thiazol-4-yl, thiazol-5-yl, 1,2,4-triazol-3-yl or tetrazol-5-yl;

5-membered partially unsaturated heterocycles, for example 4,5-dihydro-1H-pyrazol-3-yl, 4,5-dihydro-1H-pyrazol-4-yl, 4,5-dihydro-1H-pyrazol-5-yl, 4,5-dihydroisoxazol-3-yl, 4,5-dihydroisoxazol-4-yl, 4,5-dihydroisoxazol-5-yl, 4,5-dihydrooxazol-2-yl, 4,5-dihydrooxazol-2-yl, 4,5-dihydrothiazol-2-yl or 4,5-dihydroimidazol-2-yl;

5-membered saturated heterocycles, for example tetrahydrofuran-2-yl, tetrahydrofuran-3-yl, tetrahydrothien-2-yl, tetrahydrothien-3-yl, tetrahydropyrrol-2-yl, tetrahydropyrrol-3-yl, 1,3-dioxolan-2-yl, 1,3-dioxolan-4-yl, 1,3-oxathiolan-2-yl, 1,3-oxathiolan-4-yl, 1,3-oxathiolan-5-yl, 1,3-dithiolan-2-yl or 1,3-dithiolan-4-yl;

6-membered aromatic heterocycles, for example pyridin-2-yl, pyridin-3-yl, pyridin-4-yl, pyrimidin-2-yl, pyrimidin-4-yl, pyrimidin-5-yl, pyrazin-2-yl, 1,3,5-triazin-2-yl, 1,2,4-triazin-3-yl, 1,2,4-triazin-5-yl or 1,2,4-triazin-6-yl;

6-membered partially unsaturated heterocycles, for example 2H-3,4-dihydropyran-6-yl, 2H-3,4-dihydropyran-5-yl, 2H-3,4-dihydropyran-4-yl, 2H-3,4-dihydropyran-3-yl, 2H-3,4-dihydropyran-2-yl, 2H-3,4-dihydrothiopyran-6-yl, 2H-3,4-dihydrothiopyran-5-yl, 2H-3,4-dihydrothiopyran-4-yl, 2H-3,4-dihydrothiopyran-3-yl, 2H-3,4-dihydrothiopyran-2-yl, 4H-5,6-dihydro-1,3-oxazin-2-yl, 4H-5,6-dihydro-1,3-thiazin-2-yl or 3,4,5,6-tetrahydropyrimidin-2-yl;

6-membered saturated heterocycles, for example tetrahydropyran-2-yl, tetrahydropyran-3-yl, tetrahydropyran-4-yl, piperidin-2-yl, piperidin-3-yl, piperidin-4-yl, tetrahydrothiopyran-2-yl, tetrahydrothiopyran-3-yl, tetrahydrothiopyran-4-yl, 1,3-dioxan-2-yl, 1,3-dioxan-4-yl, 1,3-dioxan-5-yl, 1,3-dithian-2-yl, 1,3-dithian-4-yl, 1,3-dithian-5-yl, 1,3-oxathian-2-yl, 1,3-oxathian-4-yl, 1,3-oxathian-5-yl, tetrahydro-1,4-oxazin-2-yl, tetrahydro-1,4-oxazin-3-yl, tetrahydro-1,4-thiazin-2-yl or tetrahydro-1,4-thiazin-3-yl.

The compounds of the formula I according to the invention where Q=Q¹ are referred to as compounds of the formula Ia, compounds of the formula I where Q=Q² are referred to as Ib, compounds of the formula I where Q=Q³ are referred to as Ic and compounds of the formula I where Q=Q⁴ are referred to as Id.

With respect to the use of the compounds of the formula I according to invention as herbicides, the variables preferably have the following meaning, in each case on their own or in combination:

X is oxygen or sulfur;

in particular oxygen;

R¹, R² are hydrogen, C₁-C₆-alkyl, hydroxyl, C₁-C₆-alkoxy, C₁-C₆-alkylthio, di(C₁-C₆-alkyl)amino, where the alkyl radicals of the five last-mentioned substituents may be partially or fully halogenated and/or may carry one to three of the following groups:

nitro, cyano, C₁-C₄-alkoxy, C₁-C₄-alkylsulfonyl or C₁-C₄-alkoxycarbonyl;

in particular hydrogen, C₁-C₄-alkyl such as methyl, ethyl, propyl, 1-methylethyl, butyl, 1-methylbutyl or 2-methylbutyl, hydroxyl, C₁-C₄-alkoxy such as methoxy, ethoxy, propoxy, 1-methylethoxy, butoxy or 2-methylbutoxy, C₁-C₄-alkylthio such as methylthio, ethylthio, propylthio or 1-methylethylthio, or di(C₁-C₄-alkyl)amino such as dimethylamino, diethylamino, dipropylamino, dibutylamino, N-methyl-N-ethylamino, N-methyl-N-propylamino, N-methyl-N-butylamino, N-ethyl-N-propylamino or N-ethyl-N-butylamino; or

R¹ and R² together form a O—O(CH₂)_(m)—O—, —O—(CH₂)_(m)—S—, —S—(CH₂)_(m)—S—, —NR⁵—(CH₂)_(m)—NR⁵—, —O—(CH₂)_(m)—NR⁵—, —S—(CH₂)_(m)—NR⁵— or —(CH₂)_(p) chain which may carry one to three radicals from the following group: halogen, cyano, C₁-C₄-alkyl or C₁-C₄-alkoxycarbonyl; in particular, R¹ and R² together form a —O—(CH₂)_(m)—O, —O—(CH₂)_(m)—S—, —S—(CH₂)_(m)—S or —(CH₂)_(p) chain;

R³ is hydrogen, nitro, cyano, halogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₁-C₆-alkylthio, C₁-C₆-haloalkylthio, C₁-C₆-alkylsulfinyl, C₁-C₆-haloalkylsulfinyl, C₁-C₆-alkylsulfonyl, C₁-C₆-haloalkylsulfonyl, —P(═O)(C₁-C₄-alkyl)₂ or —P(═O)(C₁-C₄-alkoxy)₂; in particular nitro, halogen, C₁-C₄-alkyl such as methyl or ethyl, C₁-C₄-haloalkyl such as difluoromethyl or trifluoromethyl, C₁-C₄-alkoxy such as methoxy or ethoxy, C₁-C₄-haloalkoxy such as difluoromethoxy, trifluoromethoxy or chlorodifluoromethoxy, C₁-C₄-alkylthio such as methylthio or ethylthio, C₁-C₄-alkylsulfonyl such as methylsulfonyl or ethylsulfonyl, C₁-C₄-haloalkylsulfonyl such as difluoromethylsulfonyl, trifluoromethylsulfonyl or chlorodifluoromethylsulfonyl, —P(═O)(CH₃)₂, —P(═O)(CH₂CH₃)₂, —P(═O)(OCH₃)₂ or —P(═O)(OCH₂CH₃)₂;

R⁴ is halogen, such as chlorine or bromine, or C₁-C₄-alkyl, such as methyl or ethyl;

R⁵ is hydrogen or C₁-C₄-alkyl, such as methyl or ethyl;

l is 0 or 1;

m is 2, 3 or 4;

p is 4 or 5;

Q is a radical of the formula Q¹, Q², Q³ or Q⁴;

R⁶ is hydroxyl, mercapto, halogen, OR¹³, SR¹³, SO₂R¹⁴, OSO₂R¹⁴, OPOR¹⁵R¹⁶, OPR¹⁵R¹⁶, OPSR¹⁵R¹⁶, NR¹⁷R¹⁸, ONR¹⁸R¹⁹, N-bonded heterocyclyl or O—(N-bonded heterocyclyl), where the heterocyclyl radical of the two last-mentioned substituents may be partially or fully halogenated and/or may carry one to three of the following radicals:

nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy or C₁-C₄-haloalkoxy;

R⁷,R⁹,R¹¹ are hydrogen, halogen, cyano, C₁-C₆-alkyl, C₁-C₆-haloalkyl, di(C₁-C₆-alkoxy)methyl, di(C₁-C₆-alkylthio)methyl, (C₁-C₆-alkoxy)(C₁-C₆-alkylthio)methyl, hydroxyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₁-C₆-alkoxycarbonyloxy, C₁-C₆-alkylthio, C₁-C₆-haloalkylthio, C₁-C₆-alkylsulfonyl, C₁-C₆-haloalkylsulfonyl, C₁-C₆-alkylcarbonyl, C₁-C₆-haloalkylcarbonyl, C₁-C₆-alkoxycarbonyl or C₁-C₆-haloalkoxycarbonyl;

R⁸,R¹⁰,R¹² are hydrogen or C₁-C₆-alkyl;

in particular hydrogen or C₁-C₄-alkyl, such as methyl or ethyl; or

R⁷ and R⁸ or R⁹ and R¹⁰ or R¹¹ and R¹² together form a —O—(CH₂)_(u)—O—, —O—(CH₂)_(u)—S—, —S—(CH₂)_(u)—S—, —O—(CH₂)_(v)— or —S—(CH₂)_(v) chain which may be substituted by one to three radicals from the following group:

halogen, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl or C₁-C₄-alkoxycarbonyl; or

R⁷ and R⁸ or R⁹ and R¹⁰ or R¹¹ and R¹² together form a —(CH₂)_(w) chain which may be interrupted by oxygen or sulfur and/or substituted by one to four radicals from the following group:

halogen, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl or C₁-C₄-alkoxycarbonyl; or

R⁷ and R⁸ or R⁹ and R¹⁰ or R¹¹ and R¹² together with the carbon atoms to which they are attached form a carbonyl group; or

R⁷ and R⁹ or R⁹ and R¹¹ or R⁷ and R¹¹ together form a —(CH₂)_(v) chain which may be substituted by one to three radicals from the following group: halogen, C₁-C₆-alkyl, C₁-C₆-alkoxy, hydroxyl or C₁-C₆-alkoxycarbonyl;

R¹³ is C₁-C₆-alkyl, C₃-C₆-alkenyl, C₃-C₆-haloalkenyl, C₃-C₆-alkynyl, C₁-C₆-alkylcarbonyl, C₂-C₆-alkenylcarbonyl, C₃-C₆-cycloalkylcarbonyl, C₁-C₆-alkylaminocarbonyl, C₁-C₆-alkylcarbonyl-C₁-C₆-alkyl or C₁-C₆-alkoxyimino-C₁-C₆-alkyl, where the abovementioned alkyl and cycloalkyl radicals may be partially or fully halogenated and/or may carry one to three of the following groups:

cyano, C₁-C₄-alkoxy, C₁-C₄-alkylthio, C₁-C₄-alkylcarbonyl, C₁-C₄-alkoxycarbonyl, hydroxycarbonyl, di(C₁-C₄-alkyl)aminocarbonyl, C₁-C₄-alkylcarbonyloxy or C₃-C₆-cycloalkyl;

is phenyl, heterocyclyl, phenyl-C₁-C₆-alkyl, heterocyclyl-C₁-C₆-alkyl, phenylcarbonyl or heterocyclylcarbonyl, where the phenyl and the heterocyclyl radical of the 6 last-mentioned substituents may be partially or fully halogenated and/or may carry one to three of the following radicals:

nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy or C₁-C₄-haloalkoxy;

R¹⁴,R¹⁵, R¹⁶ are C₁-C₆-alkyl, C₃-C₆-alkenyl, C₃-C₆-haloalkenyl, C₃-C₆-cycloalkyl, hydroxyl, C₁-C₆-alkoxy, di(C₁-C₆-alkyl)amino or di(C₁-C₆-haloalkyl)amino, where the abovementioned alkyl, cycloalkyl and alkoxy radicals may be partially or fully halogenated and/or may carry one to three of the following groups: cyano, C₁-C₄-alkoxy, C₁-C₄-alkylthio, C₁-C₄-alkylcarbonyl or C₁-C₄-alkoxycarbonyl;

are phenyl, heterocyclyl, phenoxy or heterocyclyloxy, where the phenyl and the heterocyclyl radical of the last-mentioned substituents may be partially or fully halogenated and/or may carry one to three of the following radicals:

nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy or C₁-C₄-haloalkoxy;

R¹⁷ is C₁-C₆-alkyl, C₃-C₆-alkenyl, C₃-C₆-haloalkenyl, C₃-C₆-cycloalkyl, C₁-C₆-alkoxy or C₃-C₆-alkenyloxy, where the abovementioned alkyl, cycloalkyl and alkoxy radicals may be partially or fully halogenated and/or may carry one to three radicals from the following group:

cyano, C₁-C₄-alkoxy or C₁-C₄-alkylthio;

is phenyl, heterocyclyl, phenyl-C₁-C₆-alkyl or heterocyclyl-C₁-C₆-alkyl, where the phenyl or heterocyclyl radical of the four last-mentioned substituents may be partially or fully halogenated and/or may carry one to three of the following radicals:

nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy or C₁-C₄-haloalkoxy;

R¹⁸, R¹⁹ are C₁-C₆-alkyl or C₃-C₆-alkenyl;

u is from 2 to 4;

v is from 1 to 5;

w is from 2 to 5;

R²⁰ is a radical as mentioned under R⁶;

R²¹ is hydrogen, C₁-C₆-alkyl or C₁-C₆-haloalkyl; in particular hydrogen or C₁-C₄-alkyl such as methyl, ethyl, propyl, 1-methyleth-1-yl or 1,1-dimethyleth-1-yl;

R²² is hydrogen or C₁-C₆-alkyl; in particular hydrogen or C₁-C₄-alkyl, such as methyl or ethyl;

R²³ is C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₃-C₆-cycloalkyl or C₃-C₆-halocycloalkyl; in particular C₁-C₆-alkyl or C₃-C₆-cycloalkyl; very preferably cyclopropyl;

R²⁴ is hydrogen;

R²⁵ is C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₃-C₆-cycloalkyl or C₃-C₆-halocycloalkyl; in particular C₁-C₆-alkyl or C₃-C₆-cycloalkyl.

Particular preference is given to the compounds Ia especially the compounds Ia where the variables have the following meanings, in each case on their own or in combination:

R⁶ is hydroxyl, mercapto, halogen, OR¹³, SR¹³, SO₂R¹⁴, OSO₂R¹⁴, NR¹⁷R¹⁸, ONR¹⁸R¹⁹ or N-bonded heterocyclyl, where the heterocyclyl radical of the last-mentioned substituent may be partially or fully halogenated and/or may carry one to three of the following radicals:

nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy or C₁-C₄-haloalkoxy;

R⁷,R⁹,R¹¹ are hydrogen, halogen, cyano, C₁-C₆-alkyl, C₁-C₆-haloalkyl, di(C₁-C₆-alkoxy)methyl, di(C₁-C₆-alkylthio)methyl, (C₁-C₆-alkoxy)(C₁-C₆-alkylthio)methyl, hydroxyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₁-C₆-alkoxycarbonyloxy, C₁-C₆-alkylthio or C₁-C₆-haloalkylthio;

R⁸,R¹⁰,R¹² are hydrogen or C₁-C₆-alkyl;

in particular hydrogen or C₁-C₄-alkyl, such as methyl or ethyl; or

R⁹ and R¹⁰ together with the carbon to which they are attached form a carbonyl group; or

R⁷ and R¹¹ together form a —(CH₂)_(v) chain which may be substituted by one to three C₁-C₄-alkyl radicals;

R¹³ is C₁-C₆-alkyl, C₃-C₆-alkenyl, C₃-C₆-haloalkenyl, C₃-C₆-alkynyl, C₁-C₆-alkylcarbonyl, C₃-C₆-cycloalkylcarbonyl, C₁-C₆-alkylaminocarbonyl or C₁-C₆-alkylcarbonyl-C₁-C₆-alkyl, where the abovementioned alkyl or cycloalkyl radicals may be partially or fully halogenated and/or may carry one to three of the following groups:

cyano, C₁-C₄-alkoxy, C₁-C₄-alkylthio, C₁-C₄-alkylcarbonyl, C₁-C₄-alkoxycarbonyl, hydroxycarbonyl, di(C₁-C₄-alkyl)aminocarbonyl, C₁-C₄-alkylcarbonyloxy or C₃-C₆-cycloalkyl;

is phenyl, heterocyclyl, phenyl-C₁-C₆-alkyl, heterocyclyl-C₁-C₆-alkyl, phenylcarbonyl or heterocyclylcarbonyl, where the phenyl and the heterocyclyl radical of the 6 last-mentioned substituents may be partially or fully halogenated and/or may carry one to three of the following radicals:

nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy or C₁-C₄-haloalkoxy;

R¹⁴ is C₁-C₆-alkyl, C₃-C₆-alkenyl, C₃-C₆-haloalkenyl, C₃-C₆-cycloalkyl, hydroxyl, C₁-C₆-alkoxy, di(C₁-C₆-alkyl)amino or di(C₁-C₆-haloalkyl)amino, where the abovementioned alkyl, cycloalkyl and alkoxy radicals may be partially or fully halogenated and/or may carry one to three of the following groups:

cyano, C₁-C₄-alkoxy, C₁-C₄-alkylthio, C₁-C₄-alkylcarbonyl or C₁-C₄-alkoxycarbonyl;

are phenyl, heterocyclyl, phenoxy or heterocyclyloxy, where the phenyl and the heterocyclyl radical of the last-mentioned substituents may be partially or fully halogenated and/or carry one to three of the following radicals:

nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy or C₁-C₄-haloalkoxy;

R¹⁷ is C₁-C₆-alkyl, C₃-C₆-alkenyl, C₃-C₆-haloalkenyl, C₃-C₆-cycloalkyl, C₁-C₆-alkoxy or C₃-C₆-alkenyloxy, where the abovementioned alkyl, cycloalkyl and alkoxy radicals may be partially or fully halogenated and/or may carry one to three radicals from the following group:

cyano, C₁-C₄-alkoxy or C₁-C₄-alkylthio;

is phenyl, heterocyclyl, phenyl-C₁-C₆-alkyl or heterocyclyl-C₁-C₆-alkyl, where the phenyl or heterocyclyl radical of the four last-mentioned substituents may be partially or fully halogenated and/or may carry one to three of the following radicals:

nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy or C₁-C₄-haloalkoxy;

R¹⁸, R¹⁹ are C₁-C₆-alkyl or C₃-C₆-alkenyl;

v is 1 or 2;

in particular 2.

Particular preference is also given to compounds of the formula Ia where

R⁶ is hydroxyl, mercapto, phenylcarbonyloxy, C₁-C₆-alkylthio, phenylthio, N—(C₁-C₆-alkoxy)-N—(C₁-C₆-alkyl)amino, 1-tetrahydropyrrolyl or 2-tetrahydroisoxazolyl, where the phenyl radicals of the abovementioned radicals may be partially or fully halogenated and/or may carry one to three of the following radicals:

nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy or C₁-C₄-haloalkoxy;

in particular hydroxyl, phenylcarbonyloxy, C₁-C₄-alkylthio, phenylthio, N—(C₁-C₄-alkoxy)-N—(C₁-C₄-alkyl)amino, 1-tetrahydropyrrolyl or 2-tetrahydroisoxazolyl;

R⁷,R⁸,R⁹,R¹⁰,R¹¹,R¹² are hydrogen or C₁-C₄-alkyl, such as methyl or ethyl;

in particular hydrogen or methyl; or

R⁹ and R¹⁰ together with the carbon to which they are attached form a carbonyl group; or

R⁷ and R¹¹ together form a —(CH₂)— or —(CH₂)₂— chain.

Extraordinary preference is given to the compounds of the formula Ia where

R⁶ is hydroxyl, mercapto, phenylcarbonyloxy, C₁-C₆-alkylthio, phenylthio, where the phenyl radicals of the abovementioned radicals may be partially or fully halogenated and/or may carry one to three of the following radicals:

nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy or C₁-C₄-haloalkoxy;

in particular hydroxyl or phenylthio, where the phenyl radical may be partially or fully halogenated and/or may carry one to three of the following radicals:

nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy or C₁-C₄-haloalkoxy.

Preference is also given to compounds Ib, especially compounds Ib where the variables have the following meanings:

R²⁰ is a radical as mentioned under R⁶;

R²¹ is hydrogen, C₁-C₆-alkyl or C₁-C₆-haloalkyl; in particular C₁-C₄-alkyl, such as methyl, ethyl, 1-methyleth-1-yl or 1,1-dimethyleth-1-yl, or C₁-C₄-haloalkyl, such as 2-fluoroethyl or 2,2,2-trifluoroethyl;

R²² is hydrogen, C₁-C₆-alkyl or C₁-C₆-haloalkyl, in particular hydrogen, C₁-C₄-alkyl, such as methyl or ethyl, or C₁-C₄-haloalkyl, such as trifluoromethyl; in particular hydrogen, methyl or trifluoromethyl.

Preference is also given to the compounds Ib where the variables have the following meanings:

R²⁰ is hydroxyl, mercapto, halogen, OR¹³, SR¹³, SO₂R¹⁴, OSO₂R¹⁴, NR¹⁷R¹⁸, ONR¹⁸R¹⁹ or N-bonded heterocyclyl, where the heterocyclyl radical of the lastmentioned substituent may be partially or fully halogenated and/or may carry one to three of the following radicals: nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy or C₁-C₄-haloalkoxy;

R¹³ is C₁-C₆-alkyl, C₃-C₆-alkenyl, C₃-C₆-haloalkenyl, C₃-C₆-alkynyl, C₁-C₆-alkylcarbonyl, C₃-C₆-cycloalkylcarbonyl, C₁-C₆-alkylaminocarbonyl, N,N-di-(C₁-C₆-alkyl) or C₁-C₆-alkylcarbonyl-C₁-C₆-alkyl, where the alkyl or cycloalkyl radicals mentioned may be partially or fully halogenated and/or may carry one to three of the following groups:

cyano, C₁ ₄-alkoxy, C₁-C₄-alkylthio, C₁-C₄-alkylcarbonyl, C₁-C₄-alkoxycarbonyl, hydroxycarbonyl, di-(C₁-C₄-alkyl)aminocarbonyl, C₁-C₄-alkylcarbonyloxy or C₃-C₆-cycloalkyl;

is phenyl, heterocyclyl, phenyl-C₁-C₆-alkyl, heterocyclyl-C₁-C₆-alkyl, phenylcarbonyl or heterocyclylcarbonyl, where the phenyl and the heterocyclyl radical of the 6 lastmentioned substituents may be partially or fully halogenated and/or may carry one to three of the following radicals:

nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy or C₁-C₄-haloalkoxy;

R¹⁴ is C₁-C₆-alkyl, C₃-C₆-alkenyl, C₃-C₆-haloalkenyl, C₃-C₆-cycloalkyl, hydroxyl, C₁-C₆-alkoxy, di-(C₁-C₆-alkyl)amino or di-(C₁-C₆-haloalkyl)amino, where the alkyl, cycloalkyl and alkoxy radicals mentioned may be partially or fully halogenated and/or may carry one to three of the following groups:

cyano, C₁-C₄-alkoxy, C₁-C₄-alkylthio, C₁-C₄-alkylcarbonyl or C₁-C₄-alkoxycarbonyl;

is phenyl, heterocyclyl, phenoxy or heterocyclyloxy, where the phenyl and the heterocyclyl radical of the lastmentioned substituents may be partially or fully halogenated and/or may carry one to three of the following radicals:

nitro, cyano, C₁-C₄-alkyl, C₁C₄-haloalkyl, C₁-C₄-alkoxy or C₁-C₄-haloalkoxy;

R¹⁷ is C₁-C₆-alkyl, C₃-C₆-alkenyl, C₃-C₆-haloalkenyl, C₃-C₆-cycloalkyl, C₁-C₆-alkoxy or C₃-C₆-alkenyloxy, where the alkyl, cycloalkyl and alkoxy radicals mentioned may be partially or fully halogenated and/or may carry one to three radicals from the group below:

cyano, C₁-C₄-alkoxy or C₁-C₄-alkylthio;

is phenyl, heterocyclyl, phenyl-C₁-C₆-alkyl or heterocyclyl-C₁-C₆-alkyl, where the phenyl or heterocyclyl radical of the four lastmentioned substituents may be partially or fully halogenated and/or may carry one to three of the following radicals:

nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy or C₁-C₄-haloalkoxy;

R¹⁸, R¹⁹ are C₁-C₆-alkyl or C₃-C₆-alkenyl;

R²¹ is C₁-C₆-alkyl, such as methyl, ethyl, 1-methyleth-1-yl, or 1,1-dimethyleth-1-yl;

R²² is hydrogen or C₁-C₆-alkyl such as methyl or ethyl; in particular hydrogen or methyl.

Extraordinary preference is given to the compounds Ib where the variables have the following meaning:

R²⁰ is hydroxyl.

Preference is also given to compounds of the formula Ic, especially compounds Ic where the variables have the following meanings:

R²³ is C₁-C₆-alkyl or C₃-C₆-cycloalkyl; in particular cyclopropyl;

R²⁴ is hydrogen.

Preference is also given to compounds of the formula Id, especially compounds Id where the variables have the following meanings:

R²⁵ is C₁-C₆-alkyl or C₃-C₆-cycloalkyl.

Preference is furthermore given to the compounds I1 (≡I where X═O, R³ is attached in the 4-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 2-position)

With respect to the variables R¹ to R⁴ and Q, what is said above applies.

Particular preference is given to the compounds I1 where the variables have the following meanings:

R³ is nitro, cyano, halogen, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₆-alkoxy, C₁-C₄-haloalkoxy, C₁-C₄-alkylsulfonyl or C₁-C₄-haloalkylsulfonyl;

R⁴ is halogen, such as chlorine or bromine, or C₁-C₄-alkyl, such as methyl or ethyl;

l is 0 or 1.

Furthermore, preference is also given to the compounds I2 (≡I where X═O, R³ is attached in the 2-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 4-position)

With respect to the variables R¹ to R⁴ and Q, what was said above applies.

Particular preference is given to the compounds I2 where the variables have the following meanings:

R³ is nitro, cyano, halogen, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₁-C₄-alkylthio, C₁-C₄-haloalkylthio, C₁-C₄-alkylsulfonyl or C₁-C₄-haloalkylsulfonyl;

R⁴ is halogen, such as chlorine or bromine, or C₁-C₄-alkyl, such as methyl or ethyl;

l is 0 or 1.

Preference is furthermore given to the compounds I, in particular the compounds Ia, Ib, I1 or I2, where the variables have the following meanings:

R¹,R² are hydrogen, hydroxyl, C₁-C₆-alkyl or C₁-C₆-alkoxy, where the alkyl radicals of the two lastmentioned substituents may be partially or fully halogenated and/or may carry one to three of the following groups: nitro, cyano, C₁-C₄-alkoxy, C₁-C₄-alkylsulfonyl or C₁-C₄-alkoxycarbonyl;

particularly preferably hydrogen, C₁-C₄-alkyl or C₁-C₄-alkoxy.

Preference is furthermore given to the compounds I1a (≡I where X═O, R³ is attached in position 4, R⁴ _(l) is attached in position 5 and “P(═X)R¹R²” is attached in position 2 and Q=Q¹).

Particular preference is given to the compounds I1a (≡I where X═O, R³ is in position 4, R⁴ _(l) is in position 5 and “P(═X)R¹R²” is in position 2), where the variables have the following meanings:

R¹,R² are C₁-C₄-alkyl or C₁-C₄-alkoxy;

in particular C₁-C₄-alkyl;

R³ is halogen;

l is 0;

R⁶ is hydroxyl;

R⁷,R⁸,R⁹,R¹⁰,R¹¹,R¹² are hydrogen or C₁-C₄-alkyl,

or R⁹ and R¹⁰ together with the carbon to which they are attached form a carbonyl group.

Preference is furthermore given to the compounds I2a (≡I where X═O, R³ is attached in position 2, R⁴ _(l) is attached in position 5 and “P(═X)R¹R²” is attached in position 4 and Q=Q¹).

Particular preference is given to the compounds I2a (≡I where X═O, R³ is attached in position 2, R⁴ _(l) is attached in position 5 and “P(═X)R¹R²” is attached in position 4 and Q=Q¹), where the variables have the following meanings:

R¹,R² are C₁-C₄-alkyl or C₁-C₄-alkoxy;

R³ is halogen;

l is 0;

R⁶ is hydroxyl or phenylthio, where the phenyl radical may be partially or fully halogenated and/or may carry one to three of the following radicals:

nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy or C₁-C₄-haloalkoxy;

R⁷,R⁸,R⁹,R¹⁰,R¹¹,R¹² are hydrogen or C₁-C₄-alkyl; or R⁹ and R¹⁰ together with the carbon to which they are attached form a carbonyl group;

or R⁷ and R¹¹ together form a —(CH₂)— or —(CH₂)₂— chain, in particular a —(CH₂)₂— chain.

Preference is furthermore given to the compounds I2b (≡I where X═O, R³ is in position 2, R⁴ _(l) is in position 5 and “P(═X)R¹R²” is in position 4).

Particular preference is given to the compounds I2b (≡I where X═O, R³ is in position 2, R⁴ _(l) is in position 5 and “P(═X)R¹R²” is in position 4), where the variables have the following meanings:

R¹,R² are C₁-C₄-alkyl or C₁-C₄-alkoxy; in particular C₁-C₄-alkoxy;

R³ is halogen;

l is 0;

R²⁰ is hydroxyl;

R²¹ is C₁-C₄-alkyl;

R²² is hydrogen or C₁-C₄-alkyl; in particular hydrogen.

Extraordinary preference is given to the compounds I1a1 (≡I where X═O, R³ is attached in the 4-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 2-position, Q=Q¹, R⁷ to R¹²=hydrogen), in particular to the compounds I1a1.n where the variables R¹ to R⁴ and R⁶ are as defined in Table 1.

The given radical definitions X, R¹ to R¹², Q and l are preferred for the compounds according to the invention not only in combination with one another, but in each case also on their own.

TABLE 1 I1a1

n R¹ R² R³ R⁴ R⁶ 1 H H H H(l = O) OH 2 CH₃ CH₃ H H(l = O) OH 3 CH₂CH₃ CH₂CH₃ H H(l = O) OH 4 CH₂CH₂CH₃ CH₂CH₂CH₃ H H(l = O) OH 5 OCH₃ OCH₃ H H(l = O) OH 6 OCH₂CH₃ OCH₂CH₃ H H(l = O) OH 7 OCH₂CH₂CH₃ OCH₂CH₂CH₃ H H(l = O) OH 8 SCH₃ SCH₃ H H(l = O) OH 9 SCH₂CH₃ SCH₂CH₃ H H(l = O) OH 10 N(CH₃)₂ N(CH₃)₂ H H(l = O) OH 11 N(CH₂CH₃)₂ N(CH₂CH₃)₂ H H(l = O) OH 12 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) H H(l = O) OH 13 O—(CH₂CH₂)—O H H(l = O) OH 14 O—(CH₂CH₂CH₂)—O H H(l = O) OH 15 S—(CH₂CH₂)—S H H(l = O) OH 16 S—(CH₂CH₂CH₂)—S H H(l = O) OH 17 —(CH₂)₄— H H(l = O) OH 18 —(CH₂)₅— H H(l = O) OH 19 H H NO₂ H(l = O) OH 20 CH₃ CH₃ NO₂ H(l = O) OH 21 CH₂CH₃ CH₂CH₃ NO₂ H(l = O) OH 22 CH₂CH₂CH₃ CH₂CH₂CH₃ NO₂ H(l = O) OH 23 OCH₃ OCH₃ NO₂ H(l = O) OH 24 OCH₂CH₃ OCH₂CH₃ NO₂ H(l = O) OH 25 OCH₂CH₂CH₃ OCH₂CH₂CH₃ NO₂ H(l = O) OH 26 SCH₃ SCH₃ NO₂ H(l = O) OH 27 SCH₂CH₃ SCH₂CH₃ NO₂ H(l = O) OH 28 N(CH₃)₂ N(CH₃)₂ NO₂ H(l = O) OH 29 N(CH₂CH₃)₂ N(CH₂CH₃)₂ NO₂ H(l = O) OH 30 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) NO₂ H(l = O) OH 31 O—(CH₂CH₂)—O NO₂ H(l = O) OH 32 O—(CH₂CH₂CH₂)—O NO₂ H(l = O) OH 33 S—(CH₂CH₂)—S NO₂ H(l = O) OH 34 S—(CH₂CH₂CH₂)—S NO₂ H(l = O) OH 35 —(CH₂)₄— NO₂ H(l = O) OH 36 —(CH₂)₅— NO₂ H(l = O) OH 37 H H CN H(l = O) OH 38 CH₃ CH₃ CN H(l = O) OH 39 CH₂CH₃ CH₂CH₃ CN H(l = O) OH 40 CH₂CH₂CH₃ CH₂CH₂CH₃ CN H(l = O) OH 41 OCH₃ OCH₃ CN H(l = O) OH 42 OCH₂CH₃ OCH₂CH₃ CN H(l = O) OH 43 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CN H(l = O) OH 44 SCH₃ SCH₃ CN H(l = O) OH 45 SCH₂CH₃ SCH₂CH₃ CN H(l = O) OH 46 N(CH₃)₂ N(CH₃)₂ CN H(l = O) OH 47 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CN H(l = O) OH 48 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CN H(l = O) OH 49 O—(CH₂CH₂)—O CN H(l = O) OH 50 O—(CH₂CH₂CH₂)—O CN H(l = O) OH 51 S—(CH₂CH₂)—S CN H(l = O) OH 52 S—(CH₂CH₂CH₂)—S CN H(l = O) OH 53 —(CH₂)₄— CN H(l = O) OH 54 —(CH₂)₅— CN H(l = O) OH 55 H H F H(l = O) OH 56 CH₃ CH₃ F H(l = O) OH 57 CH₂CH₃ CH₂CH₃ F H(l = O) OH 58 CH₂CH₂CH₃ CH₂CH₂CH₃ F H(l = O) OH 59 OCH₃ OCH₃ F H(l = O) OH 60 OCH₂CH₃ OCH₂CH₃ F H(l = O) OH 61 OCH₂CH₂CH₃ OCH₂CH₂CH₃ F H(l = O) OH 62 SCH₃ SCH₃ F H(l = O) OH 63 SCH₂CH₃ SCH₂CH₃ F H(l = O) OH 64 N(CH₃)₂ N(CH₃)₂ F H(l = O) OH 65 N(CH₂CH₃)₂ N(CH₂CH₃)₂ F H(l = O) OH 66 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) F H(l = O) OH 67 O—(CH₂CH₂)—O F H(l = O) OH 68 O—(CH₂CH₂CH₂)—O F H(l = O) OH 69 S—(CH₂CH₂)—S F H(l = O) OH 70 S—(CH₂CH₂CH₂)—S F H(l = O) OH 71 —(CH₂)₄— F H(l = O) OH 72 —(CH₂)₅— F H(l = O) OH 73 H H Cl H(l = O) OH 74 CH₃ CH₃ Cl H(l = O) OH 75 CH₂CH₃ CH₂CH₃ Cl H(l = O) OH 76 CH₂CH₂CH₃ CH₂CH₂CH₃ Cl H(l = O) OH 77 OCH₃ OCH₃ Cl H(l = O) OH 78 OCH₂CH₃ OCH₂CH₃ Cl H(l = O) OH 79 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Cl H(l = O) OH 80 SCH₃ SCH₃ Cl H(l = O) OH 81 SCH₂CH₃ SCH₂CH₃ Cl H(l = O) OH 82 N(CH₃)₂ N(CH₃)₂ Cl H(l = O) OH 83 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Cl H(l = O) OH 84 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Cl H(l = O) OH 85 O—(CH₂CH₂)—O Cl H(l = O) OH 86 O—(CH₂CH₂CH₂)—O Cl H(l = O) OH 87 S—(CH₂CH₂)—S Cl H(l = O) OH 88 S—(CH₂CH₂CH₂)—S Cl H(l = O) OH 89 —(CH₂)₄— Cl H(l = O) OH 90 —(CH₂)₅— Cl H(l = O) OH 91 H H Br H(l = O) OH 92 CH₃ CH₃ Br H(l = O) OH 93 CH₂CH₃ CH₂CH₃ Br H(l = O) OH 94 CH₂CH₂CH₃ CH₂CH₂CH₃ Br H(l = O) OH 95 OCH₃ OCH₃ Br H(l = O) OH 96 OCH₂CH₃ OCH₂CH₃ Br H(l = O) OH 97 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Br H(l = O) OH 98 SCH₃ SCH₃ Br H(l = O) OH 99 SCH₂CH₃ SCH₂CH₃ Br H(l = O) OH 100 N(CH₃)₂ N(CH₃)₂ Br H(l = O) OH 101 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Br H(l = O) OH 102 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Br H(l = O) OH 103 O—(CH₂CH₂)—O Br H(l = O) OH 104 O—(CH₂CH₂CH₂)—O Br H(l = O) OH 105 S—(CH₂CH₂)—S Br H(l = O) OH 106 S—(CH₂CH₂CH₂)—S Br H(l = O) OH 107 —(CH₂)₄— Br H(l = O) OH 108 —(CH₂)₅— Br H(l = O) OH 109 H H CH₃ H(l = O) OH 110 CH₃ CH₃ CH₃ H(l = O) OH 111 CH₂CH₃ CH₂CH₃ CH₃ H(l = O) OH 112 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₃ H(l = O) OH 113 OCH₃ OCH₃ CH₃ H(l = O) OH 114 OCH₂CH₃ OCH₂CH₃ CH₃ H(l = O) OH 115 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₃ H(l = O) OH 116 SCH₃ SCH₃ CH₃ H(l = O) OH 117 SCH₂CH₃ SCH₂CH₃ CH₃ H(l = O) OH 118 N(CH₃)₂ N(CH₃)₂ CH₃ H(l = O) OH 119 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₃ H(l = O) OH 120 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₃ H(l = O) OH 121 O—(CH₂CH₂)—O CH₃ H(l = O) OH 122 O—(CH₂CH₂CH₂)—O CH₃ H(l = O) OH 123 S—(CH₂CH₂)—S CH₃ H(l = O) OH 124 S—(CH₂CH₂CH₂)—S CH₃ H(l = O) OH 125 —(CH₂)₄— CH₃ H(l = O) OH 126 —(CH₂)₅— CH₃ H(l = O) OH 127 H H CH₂CH₃ H(l = O) OH 128 CH₃ CH₃ CH₂CH₃ H(l = O) OH 129 CH₂CH₃ CH₂CH₃ CH₂CH₃ H(l = O) OH 130 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₂CH₃ H(l = O) OH 131 OCH₃ OCH₃ CH₂CH₃ H(l = O) OH 132 OCH₂CH₃ OCH₂CH₃ CH₂CH₃ H(l = O) OH 133 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₂CH₃ H(l = O) OH 134 SCH₃ SCH₃ CH₂CH₃ H(l = O) OH 135 SCH₂CH₃ SCH₂CH₃ CH₂CH₃ H(l = O) OH 136 N(CH₃)₂ N(CH₃)₂ CH₂CH₃ H(l = O) OH 137 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₂CH₃ H(l = O) OH 138 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₂CH₃ H(l = O) OH 139 O—(CH₂CH₂)—O CH₂CH₃ H(l = O) OH 140 O—(CH₂CH₂CH₂)—O CH₂CH₃ H(l = O) OH 141 S—(CH₂CH₂)—S CH₂CH₃ H(l = O) OH 142 S—(CH₂CH₂CH₂)—S CH₂CH₃ H(l = O) OH 143 —(CH₂)₄— CH₂CH₃ H(l = O) OH 144 —(CH₂)₅— CH₂CH₃ H(l = O) OH 145 H H CF₃ H(l = O) OH 146 CH₃ CH₃ CF₃ H(l = O) OH 147 CH₂CH₃ CH₂CH₃ CF₃ H(l = O) OH 148 CH₂CH₂CH₃ CH₂CH₂CH₃ CF₃ H(l = O) OH 149 OCH₃ OCH₃ CF₃ H(l = O) OH 150 OCH₂CH₃ OCH₂CH₃ CF₃ H(l = O) OH 151 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CF₃ H(l = O) OH 152 SCH₃ SCH₃ CF₃ H(l = O) OH 153 SCH₂CH₃ SCH₂CH₃ CF₃ H(l = O) OH 154 N(CH₃)₂ N(CH₃)₂ CF₃ H(l = O) OH 155 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CF₃ H(l = O) OH 156 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CF₃ H(l = O) OH 157 O—(CH₂CH₂)—O CF₃ H(l = O) OH 158 O—(CH₂CH₂CH₂)—O CF₃ H(l = O) OH 159 S—(CH₂CH₂)—S CF₃ H(l = O) OH 160 S—(CH₂CH₂CH₂)—S CF₃ H(l = O) OH 161 —(CH₂)₄— CF₃ H(l = O) OH 162 —(CH₂)₅— CF₃ H(l = O) OH 163 H H OCH₃ H(l = O) OH 164 CH₃ CH₃ OCH₃ H(l = O) OH 165 CH₂CH₃ CH₂CH₃ OCH₃ H(l = O) OH 166 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₃ H(l = O) OH 167 OCH₃ OCH₃ OCH₃ H(l = O) OH 168 OCH₂CH₃ OCH₂CH₃ OCH₃ H(l = O) OH 169 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₃ H(l = O) OH 170 SCH₃ SCH₃ OCH₃ H(l = O) OH 171 SCH₂CH₃ SCH₂CH₃ OCH₃ H(l = O) OH 172 N(CH₃)₂ N(CH₃)₂ OCH₃ H(l = O) OH 173 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₃ H(l = O) OH 174 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₃ H(l = O) OH 175 O—(CH₂CH₂)—O OCH₃ H(l = O) OH 176 O—(CH₂CH₂CH₂)—O OCH₃ H(l = O) OH 177 S—(CH₂CH₂)—S OCH₃ H(l = O) OH 178 S—(CH₂CH₂CH₂)—S OCH₃ H(l = O) OH 179 —(CH₂)₄— OCH₃ H(l = O) OH 180 —(CH₂)₅— OCH₃ H(l = O) OH 181 H H OCH₂CH₃ H(l = O) OH 182 CH₃ CH₃ OCH₂CH₃ H(l = O) OH 183 CH₂CH₃ CH₂CH₃ OCH₂CH₃ H(l = O) OH 184 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₂CH₃ H(l = O) OH 185 OCH₃ OCH₃ OCH₂CH₃ H(l = O) OH 186 OCH₂CH₃ OCH₂CH₃ OCH₂CH₃ H(l = O) OH 187 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₂CH₃ H(l = O) OH 188 SCH₃ SCH₃ OCH₂CH₃ H(l = O) OH 189 SCH₂CH₃ SCH₂CH₃ OCH₂CH₃ H(l = O) OH 190 N(CH₃)₂ N(CH₃)₂ OCH₂CH₃ H(l = O) OH 191 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₂CH₃ H(l = O) OH 192 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₂CH₃ H(l = O) OH 193 O—(CH₂CH₂)—O OCH₂CH₃ H(l = O) OH 194 O—(CH₂CH₂CH₂)—O OCH₂CH₃ H(l = O) OH 195 S—(CH₂CH₂)—S OCH₂CH₃ H(l = O) OH 196 S—(CH₂CH₂CH₂)—S OCH₂CH₃ H(l = O) OH 197 —(CH₂)₄— OCH₂CH₃ H(l = O) OH 198 —(CH₂)₅— OCH₂CH₃ H(l = O) OH 199 H H SCH₃ H(l = O) OH 200 CH₃ CH₃ SCH₃ H(l = O) OH 201 CH₂CH₃ CH₂CH₃ SCH₃ H(l = O) OH 202 CH₂CH₂CH₃ CH₂CH₂CH₃ SCH₃ H(l = O) OH 203 OCH₃ OCH₃ SCH₃ H(l = O) OH 204 OCH₂CH₃ OCH₂CH₃ SCH₃ H(l = O) OH 205 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SCH₃ H(l = O) OH 206 SCH₃ SCH₃ SCH₃ H(l = O) OH 207 SCH₂CH₃ SCH₂CH₃ SCH₃ H(l = O) OH 208 N(CH₃)₂ N(CH₃)₂ SCH₃ H(l = O) OH 209 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SCH₃ H(l = O) OH 210 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SCH₃ H(l = O) OH 211 O—(CH₂CH₂)—O SCH₃ H(l = O) OH 212 O—(CH₂CH₂CH₂)—O SCH₃ H(l = O) OH 213 S—(CH₂CH₂)—S SCH₃ H(l = O) OH 214 S—(CH₂CH₂CH₂)—S SCH₃ H(l = O) OH 215 —(CH₂)₄— SCH₃ H(l = O) OH 216 —(CH₂)₅— SCH₃ H(l = O) OH 217 H H SO₂CH₃ H(l = O) OH 218 CH₃ CH₃ SO₂CH₃ H(l = O) OH 219 CH₂CH₃ CH₂CH₃ SO₂CH₃ H(l = O) OH 220 CH₂CH₂CH₃ CH₂CH₂CH₃ SO₂CH₃ H(l = O) OH 221 OCH₃ OCH₃ SO₂CH₃ H(l = O) OH 222 OCH₂CH₃ OCH₂CH₃ SO₂CH₃ H(l = O) OH 223 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SO₂CH₃ H(l = O) OH 224 SCH₃ SCH₃ SO₂CH₃ H(l = O) OH 225 SCH₂CH₃ SCH₂CH₃ SO₂CH₃ H(l = O) OH 226 N(CH₃)₂ N(CH₃)₂ SO₂CH₃ H(l = O) OH 227 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SO₂CH₃ H(l = O) OH 228 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SO₂CH₃ H(l = O) OH 229 O—(CH₂CH₂)—O SO₂CH₃ H(l = O) OH 230 O—(CH₂CH₂CH₂)—O SO₂CH₃ H(l = O) OH 231 S—(CH₂CH₂)—S SO₂CH₃ H(l = O) OH 232 S—(CH₂CH₂CH₂)—S SO₂CH₃ H(l = O) OH 233 —(CH₂)₄— SO₂CH₃ H(l = O) OH 234 —(CH₂)₅— SO₂CH₃ H(l = O) OH 235 H H PO(OCH₃)₂ H(l = O) OH 236 CH₃ CH₃ PO(OCH₃)₂ H(l = O) OH 237 CH₂CH₃ CH₂CH₃ PO(OCH₃)₂ H(l = O) OH 238 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₃)₂ H(l = O) OH 239 OCH₃ OCH₃ PO(OCH₃)₂ H(l = O) OH 240 OCH₂CH₃ OCH₂CH₃ PO(OCH₃)₂ H(l = O) OH 241 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₃)₂ H(l = O) OH 242 SCH₃ SCH₃ PO(OCH₃)₂ H(l = O) OH 243 SCH₂CH₃ SCH₂CH₃ PO(OCH₃)₂ H(l = O) OH 244 N(CH₃)₂ N(CH₃)₂ PO(OCH₃)₂ H(l = O) OH 245 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₃)₂ H(l = O) OH 246 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₃)₂ H(l = O) OH 247 O—(CH₂CH₂)—O PO(OCH₃)₂ H(l = O) OH 248 O—(CH₂CH₂CH₂)—O PO(OCH₃)₂ H(l = O) OH 249 S—(CH₂CH₂)—S PO(OCH₃)₂ H(l = O) OH 250 S—(CH₂CH₂CH₂)—S PO(OCH₃)₂ H(l = O) OH 251 —(CH₂)₄— PO(OCH₃)₂ H(l = O) OH 252 —(CH₂)₅— PO(OCH₃)₂ H(l = O) OH 253 H H PO(OCH₂CH₃)₂ H(l = O) OH 254 CH₃ CH₃ PO(OCH₂CH₃)₂ H(l = O) OH 255 CH₂CH₃ CH₂CH₃ PO(OCH₂CH₃)₂ H(l = O) OH 256 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₂CH₃)₂ H(l = O) OH 257 OCH₃ OCH₃ PO(OCH₂CH₃)₂ H(l = O) OH 258 OCH₂CH₃ OCH₂CH₃ PO(OCH₂CH₃)₂ H(l = O) OH 259 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₂CH₃)₂ H(l = O) OH 260 SCH₃ SCH₃ PO(OCH₂CH₃)₂ H(l = O) OH 261 SCH₂CH₃ SCH₂CH₃ PO(OCH₂CH₃)₂ H(l = O) OH 262 N(CH₃)₂ N(CH₃)₂ PO(OCH₂CH₃)₂ H(l = O) OH 263 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₂CH₃)₂ H(l = O) OH 264 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₂CH₃)₂ H(l = O) OH 265 O—(CH₂CH₂)—O PO(OCH₂CH₃)₂ H(l = O) OH 266 O—(CH₂CH₂CH₂)—O PO(OCH₂CH₃)₂ H(l = O) OH 267 S—(CH₂CH₂)—S PO(OCH₂CH₃)₂ H(l = O) OH 268 S—(CH₂CH₂CH₂)—S PO(OCH₂CH₃)₂ H(l = O) OH 269 —(CH₂)₄— PO(OCH₂CH₃)₂ H(l = O) OH 270 —(CH₂)₅— PO(OCH₂CH₃)₂ H(l = O) OH 271 H H PO(CH₃)₂ H(l = O) OH 272 CH₃ CH₃ PO(CH₃)₂ H(l = O) OH 273 CH₂CH₃ CH₂CH₃ PO(CH₃)₂ H(l = O) OH 274 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₃)₂ H(l = O) OH 275 OCH₃ OCH₃ PO(CH₃)₂ H(l = O) OH 276 OCH₂CH₃ OCH₂CH₃ PO(CH₃)₂ H(l = O) OH 277 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₃)₂ H(l = O) OH 278 SCH₃ SCH₃ PO(CH₃)₂ H(l = O) OH 279 SCH₂CH₃ SCH₂CH₃ PO(CH₃)₂ H(l = O) OH 280 N(CH₃)₂ N(CH₃)₂ PO(CH₃)₂ H(l = O) OH 281 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₃)₂ H(l = O) OH 282 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₃)₂ H(l = O) OH 283 O—(CH₂CH₂)—O PO(CH₃)₂ H(l = O) OH 284 O—(CH₂CH₂CH₂)—O PO(CH₃)₂ H(l = O) OH 285 S—(CH₂CH₂)—S PO(CH₃)₂ H(l = O) OH 286 S—(CH₂CH₂CH₂)—S PO(CH₃)₂ H(l = O) OH 287 —(CH₂)₄— PO(CH₃)₂ H(l = O) OH 288 —(CH₂)₅— PO(CH₃)₂ H(l = O) OH 289 H H PO(CH₂CH₃)₂ H(l = O) OH 290 CH₃ CH₃ PO(CH₂CH₃)₂ H(l = O) OH 291 CH₂CH₃ CH₂CH₃ PO(CH₂CH₃)₂ H(l = O) OH 292 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₂CH₃)₂ H(l = O) OH 293 OCH₃ OCH₃ PO(CH₂CH₃)₂ H(l = O) OH 294 OCH₂CH₃ OCH₂CH₃ PO(CH₂CH₃)₂ H(l = O) OH 295 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₂CH₃)₂ H(l = O) OH 296 SCH₃ SCH₃ PO(CH₂CH₃)₂ H(l = O) OH 297 SCH₂CH₃ SCH₂CH₃ PO(CH₂CH₃)₂ H(l = O) OH 298 N(CH₃)₂ N(CH₃)₂ PO(CH₂CH₃)₂ H(l = O) OH 299 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₂CH₃)₂ H(l = O) OH 300 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₂CH₃)₂ H(l = O) OH 301 O—(CH₂CH₂)—O PO(CH₂CH₃)₂ H(l = O) OH 302 O—(CH₂CH₂CH₂)—O PO(CH₂CH₃)₂ H(l = O) OH 303 S—(CH₂CH₂)—S PO(CH₂CH₃)₂ H(l = O) OH 304 S—(CH₂CH₂CH₂)—S PO(CH₂CH₃)₂ H(l = O) OH 305 —(CH₂)₄— PO(CH₂CH₃)₂ H(l = O) OH 306 —(CH₂)₅— PO(CH₂CH₃)₂ H(l = O) OH 307 H H H H(l = O) OCOC₆H₅ 308 CH₃ CH₃ H H(l = O) OCOC₆H₅ 309 CH₂CH₃ CH₂CH₃ H H(l = O) OCOC₆H₅ 310 CH₂CH₂CH₃ CH₂CH₂CH₃ H H(l = O) OCOC₆H₅ 311 OCH₃ OCH₃ H H(l = O) OCOC₆H₅ 312 OCH₂CH₃ OCH₂CH₃ H H(l = O) OCOC₆H₅ 313 OCH₂CH₂CH₃ OCH₂CH₂CH₃ H H(l = O) OCOC₆H₅ 314 SCH₃ SCH₃ H H(l = O) OCOC₆H₅ 315 SCH₂CH₃ SCH₂CH₃ H H(l = O) OCOC₆H₅ 316 N(CH₃)₂ N(CH₃)₂ H H(l = O) OCOC₆H₅ 317 N(CH₂CH₃)₂ N(CH₂CH₃)₂ H H(l = O) OCOC₆H₅ 318 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) H H(l = O) OCOC₆H₅ 319 O—(CH₂CH₂)—O H H(l = O) OCOC₆H₅ 320 O—(CH₂CH₂CH₂)—O H H(l = O) OCOC₆H₅ 321 S—(CH₂CH₂)—S H H(l = O) OCOC₆H₅ 322 S—(CH₂CH₂CH₂)—S H H(l = O) OCOC₆H₅ 323 —(CH₂)₄— H H(l = O) OCOC₆H₅ 324 —(CH₂)₅— H H(l = O) OCOC₆H₅ 325 H H NO₂ H(l = O) OCOC₆H₅ 326 CH₃ CH₃ NO₂ H(l = O) OCOC₆H₅ 327 CH₂CH₃ CH₂CH₃ NO₂ H(l = O) OCOC₆H₅ 328 CH₂CH₂CH₃ CH₂CH₂CH₃ NO₂ H(l = O) OCOC₆H₅ 329 OCH₃ OCH₃ NO₂ H(l = O) OCOC₆H₅ 330 OCH₂CH₃ OCH₂CH₃ NO₂ H(l = O) OCOC₆H₅ 331 OCH₂CH₂CH₃ OCH₂CH₂CH₃ NO₂ H(l = O) OCOC₆H₅ 332 SCH₃ SCH₃ NO₂ H(l = O) OCOC₆H₅ 333 SCH₂CH₃ SCH₂CH₃ NO₂ H(l = O) OCOC₆H₅ 334 N(CH₃)₂ N(CH₃)₂ NO₂ H(l = O) OCOC₆H₅ 335 N(CH₂CH₃)₂ N(CH₂CH₃)₂ NO₂ H(l = O) OCOC₆H₅ 336 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) NO₂ H(l = O) OCOC₆H₅ 337 O—(CH₂CH₂)—O NO₂ H(l = O) OCOC₆H₅ 338 O—(CH₂CH₂CH₂)—O NO₂ H(l = O) OCOC₆H₅ 339 S—(CH₂CH₂)—S NO₂ H(l = O) OCOC₆H₅ 340 S—(CH₂CH₂CH₂)—S NO₂ H(l = O) OCOC₆H₅ 341 —(CH₂)₄— NO₂ H(l = O) OCOC₆H₅ 342 —(CH₂)₅— NO₂ H(l = O) OCOC₆H₅ 343 H H CN H(l = O) OCOC₆H₅ 344 CH₃ CH₃ CN H(l = O) OCOC₆H₅ 345 CH₂CH₃ CH₂CH₃ CN H(l = O) OCOC₆H₅ 346 CH₂CH₂CH₃ CH₂CH₂CH₃ CN H(l = O) OCOC₆H₅ 347 OCH₃ OCH₃ CN H(l = O) OCOC₆H₅ 348 OCH₂CH₃ OCH₂CH₃ CN H(l = O) OCOC₆H₅ 349 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CN H(l = O) OCOC₆H₅ 350 SCH₃ SCH₃ CN H(l = O) OCOC₆H₅ 351 SCH₂CH₃ SCH₂CH₃ CN H(l = O) OCOC₆H₅ 352 N(CH₃)₂ N(CH₃)₂ CN H(l = O) OCOC₆H₅ 353 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CN H(l = O) OCOC₆H₅ 354 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CN H(l = O) OCOC₆H₅ 355 O—(CH₂CH₂)—O CN H(l = O) OCOC₆H₅ 356 O—(CH₂CH₂CH₂)—O CN H(l = O) OCOC₆H₅ 357 S—(CH₂CH₂)—S CN H(l = O) OCOC₆H₅ 358 S—(CH₂CH₂CH₂)—S CN H(l = O) OCOC₆H₅ 359 —(CH₂)₄— CN H(l = O) OCOC₆H₅ 360 —(CH₂)₅— CN H(l = O) OCOC₆H₅ 361 H H F H(l = O) OCOC₆H₅ 362 CH₃ CH₃ F H(l = O) OCOC₆H₅ 363 CH₂CH₃ CH₂CH₃ F H(l = O) OCOC₆H₅ 364 CH₂CH₂CH₃ CH₂CH₂CH₃ F H(l = O) OCOC₆H₅ 365 OCH₃ OCH₃ F H(l = O) OCOC₆H₅ 366 OCH₂CH₃ OCH₂CH₃ F H(l = O) OCOC₆H₅ 367 OCH₂CH₂CH₃ OCH₂CH₂CH₃ F H(l = O) OCOC₆H₅ 368 SCH₃ SCH₃ F H(l = O) OCOC₆H₅ 369 SCH₂CH₃ SCH₂CH₃ F H(l = O) OCOC₆H₅ 370 N(CH₃)₂ N(CH₃)₂ F H(l = O) OCOC₆H₅ 371 N(CH₂CH₃)₂ N(CH₂CH₃)₂ F H(l = O) OCOC₆H₅ 372 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) F H(l = O) OCOC₆H₅ 373 O—(CH₂CH₂)—O F H(l = O) OCOC₆H₅ 374 O—(CH₂CH₂CH₂)—O F H(l = O) OCOC₆H₅ 375 S—(CH₂CH₂)—S F H(l = O) OCOC₆H₅ 376 S—(CH₂CH₂CH₂)—S F H(l = O) OCOC₆H₅ 377 —(CH₂)₄— F H(l = O) OCOC₆H₅ 378 —(CH₂)₅— F H(l = O) OCOC₆H₅ 379 H H Cl H(l = O) OCOC₆H₅ 380 CH₃ CH₃ Cl H(l = O) OCOC₆H₅ 381 CH₂CH₃ CH₂CH₃ Cl H(l = O) OCOC₆H₅ 382 CH₂CH₂CH₃ CH₂CH₂CH₃ Cl H(l = O) OCOC₆H₅ 383 OCH₃ OCH₃ Cl H(l = O) OCOC₆H₅ 384 OCH₂CH₃ OCH₂CH₃ Cl H(l = O) OCOC₆H₅ 385 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Cl H(l = O) OCOC₆H₅ 386 SCH₃ SCH₃ Cl H(l = O) OCOC₆H₅ 387 SCH₂CH₃ SCH₂CH₃ Cl H(l = O) OCOC₆H₅ 388 N(CH₃)₂ N(CH₃)₂ Cl H(l = O) OCOC₆H₅ 389 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Cl H(l = O) OCOC₆H₅ 390 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Cl H(l = O) OCOC₆H₅ 391 O—(CH₂CH₂)—O Cl H(l = O) OCOC₆H₅ 392 O—(CH₂CH₂CH₂)—O Cl H(l = O) OCOC₆H₅ 393 S—(CH₂CH₂)—S Cl H(l = O) OCOC₆H₅ 394 S—(CH₂CH₂CH₂)—S Cl H(l = O) OCOC₆H₅ 395 —(CH₂)₄— Cl H(l = O) OCOC₆H₅ 396 —(CH₂)₅— Cl H(l = O) OCOC₆H₅ 397 H H Br H(l = O) OCOC₆H₅ 398 CH₃ CH₃ Br H(l = O) OCOC₆H₅ 399 CH₂CH₃ CH₂CH₃ Br H(l = O) OCOC₆H₅ 400 CH₂CH₂CH₃ CH₂CH₂CH₃ Br H(l = O) OCOC₆H₅ 401 OCH₃ OCH₃ Br H(l = O) OCOC₆H₅ 402 OCH₂CH₃ OCH₂CH₃ Br H(l = O) OCOC₆H₅ 403 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Br H(l = O) OCOC₆H₅ 404 SCH₃ SCH₃ Br H(l = O) OCOC₆H₅ 405 SCH₂CH₃ SCH₂CH₃ Br H(l = O) OCOC₆H₅ 406 N(CH₃)₂ N(CH₃)₂ Br H(l = O) OCOC₆H₅ 407 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Br H(l = O) OCOC₆H₅ 408 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Br H(l = O) OCOC₆H₅ 409 O—(CH₂CH₂)—O Br H(l = O) OCOC₆H₅ 410 O—(CH₂CH₂CH₂)—O Br H(l = O) OCOC₆H₅ 411 S—(CH₂CH₂)—S Br H(l = O) OCOC₆H₅ 412 S—(CH₂CH₂CH₂)—S Br H(l = O) OCOC₆H₅ 413 —(CH₂)₄— Br H(l = O) OCOC₆H₅ 414 —(CH₂)₅— Br H(l = O) OCOC₆H₅ 415 H H CH₃ H(l = O) OCOC₆H₅ 416 CH₃ CH₃ CH₃ H(l = O) OCOC₆H₅ 417 CH₂CH₃ CH₂CH₃ CH₃ H(l = O) OCOC₆H₅ 418 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₃ H(l = O) OCOC₆H₅ 419 OCH₃ OCH₃ CH₃ H(l = O) OCOC₆H₅ 420 OCH₂CH₃ OCH₂CH₃ CH₃ H(l = O) OCOC₆H₅ 421 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₃ H(l = O) OCOC₆H₅ 422 SCH₃ SCH₃ CH₃ H(l = O) OCOC₆H₅ 423 SCH₂CH₃ SCH₂CH₃ CH₃ H(l = O) OCOC₆H₅ 424 N(CH₃)₂ N(CH₃)₂ CH₃ H(l = O) OCOC₆H₅ 425 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₃ H(l = O) OCOC₆H₅ 426 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₃ H(l = O) OCOC₆H₅ 427 O—(CH₂CH₂)—O CH₃ H(l = O) OCOC₆H₅ 428 O—(CH₂CH₂CH₂)—O CH₃ H(l = O) OCOC₆H₅ 429 S—(CH₂CH₂)—S CH₃ H(l = O) OCOC₆H₅ 430 S—(CH₂CH₂CH₂)—S CH₃ H(l = O) OCOC₆H₅ 431 —(CH₂)₄— CH₃ H(l = O) OCOC₆H₅ 432 —(CH₂)₅— CH₃ H(l = O) OCOC₆H₅ 433 H H CH₂CH₃ H(l = O) OCOC₆H₅ 434 CH₃ CH₃ CH₂CH₃ H(l = O) OCOC₆H₅ 435 CH₂CH₃ CH₂CH₃ CH₂CH₃ H(l = O) OCOC₆H₅ 436 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₂CH₃ H(l = O) OCOC₆H₅ 437 OCH₃ OCH₃ CH₂CH₃ H(l = O) OCOC₆H₅ 438 OCH₂CH₃ OCH₂CH₃ CH₂CH₃ H(l = O) OCOC₆H₅ 439 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₂CH₃ H(l = O) OCOC₆H₅ 440 SCH₃ SCH₃ CH₂CH₃ H(l = O) OCOC₆H₅ 441 SCH₂CH₃ SCH₂CH₃ CH₂CH₃ H(l = O) OCOC₆H₅ 442 N(CH₃)₂ N(CH₃)₂ CH₂CH₃ H(l = O) OCOC₆H₅ 443 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₂CH₃ H(l = O) OCOC₆H₅ 444 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₂CH₃ H(l = O) OCOC₆H₅ 445 O—(CH₂CH₂)—O CH₂CH₃ H(l = O) OCOC₆H₅ 446 O—(CH₂CH₂CH₂)—O CH₂CH₃ H(l = O) OCOC₆H₅ 447 S—(CH₂CH₂)—S CH₂CH₃ H(l = O) OCOC₆H₅ 448 S—(CH₂CH₂CH₂)—S CH₂CH₃ H(l = O) OCOC₆H₅ 449 —(CH₂)₄— CH₂CH₃ H(l = O) OCOC₆H₅ 450 —(CH₂)₅— CH₂CH₃ H(l = O) OCOC₆H₅ 451 H H CF₃ H(l = O) OCOC₆H₅ 452 CH₃ CH₃ CF₃ H(l = O) OCOC₆H₅ 453 CH₂CH₃ CH₂CH₃ CF₃ H(l = O) OCOC₆H₅ 454 CH₂CH₂CH₃ CH₂CH₂CH₃ CF₃ H(l = O) OCOC₆H₅ 455 OCH₃ OCH₃ CF₃ H(l = O) OCOC₆H₅ 456 OCH₂CH₃ OCH₂CH₃ CF₃ H(l = O) OCOC₆H₅ 457 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CF₃ H(l = O) OCOC₆H₅ 458 SCH₃ SCH₃ CF₃ H(l = O) OCOC₆H₅ 459 SCH₂CH₃ SCH₂CH₃ CF₃ H(l = O) OCOC₆H₅ 460 N(CH₃)₂ N(CH₃)₂ CF₃ H(l = O) OCOC₆H₅ 461 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CF₃ H(l = O) OCOC₆H₅ 462 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CF₃ H(l = O) OCOC₆H₅ 463 O—(CH₂CH₂)—O CF₃ H(l = O) OCOC₆H₅ 464 O—(CH₂CH₂CH₂)—O CF₃ H(l = O) OCOC₆H₅ 465 S—(CH₂CH₂)—S CF₃ H(l = O) OCOC₆H₅ 466 S—(CH₂CH₂CH₂)—S CF₃ H(l = O) OCOC₆H₅ 467 —(CH₂)₄— CF₃ H(l = O) OCOC₆H₅ 468 —(CH₂)₅— CF₃ H(l = O) OCOC₆H₅ 469 H H OCH₃ H(l = O) OCOC₆H₅ 470 CH₃ CH₃ OCH₃ H(l = O) OCOC₆H₅ 471 CH₂CH₃ CH₂CH₃ OCH₃ H(l = O) OCOC₆H₅ 472 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₃ H(l = O) OCOC₆H₅ 473 OCH₃ OCH₃ OCH₃ H(l = O) OCOC₆H₅ 474 OCH₂CH₃ OCH₂CH₃ OCH₃ H(l = O) OCOC₆H₅ 475 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₃ H(l = O) OCOC₆H₅ 476 SCH₃ SCH₃ OCH₃ H(l = O) OCOC₆H₅ 477 SCH₂CH₃ SCH₂CH₃ OCH₃ H(l = O) OCOC₆H₅ 478 N(CH₃)₂ N(CH₃)₂ OCH₃ H(l = O) OCOC₆H₅ 479 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₃ H(l = O) OCOC₆H₅ 480 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₃ H(l = O) OCOC₆H₅ 481 O—(CH₂CH₂)—O OCH₃ H(l = O) OCOC₆H₅ 482 O—(CH₂CH₂CH₂)—O OCH₃ H(l = O) OCOC₆H₅ 483 S—(CH₂CH₂)—S OCH₃ H(l = O) OCOC₆H₅ 484 S—(CH₂CH₂CH₂)—S OCH₃ H(l = O) OCOC₆H₅ 485 —(CH₂)₄— OCH₃ H(l = O) OCOC₆H₅ 486 —(CH₂)₅— OCH₃ H(l = O) OCOC₆H₅ 487 H H OCH₂CH₃ H(l = O) OCOC₆H₅ 488 CH₃ CH₃ OCH₂CH₃ H(l = O) OCOC₆H₅ 489 CH₂CH₃ CH₂CH₃ OCH₂CH₃ H(l = O) OCOC₆H₅ 490 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₂CH₃ H(l = O) OCOC₆H₅ 491 OCH₃ OCH₃ OCH₂CH₃ H(l = O) OCOC₆H₅ 492 OCH₂CH₃ OCH₂CH₃ OCH₂CH₃ H(l = O) OCOC₆H₅ 493 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₂CH₃ H(l = O) OCOC₆H₅ 494 SCH₃ SCH₃ OCH₂CH₃ H(l = O) OCOC₆H₅ 495 SCH₂CH₃ SCH₂CH₃ OCH₂CH₃ H(l = O) OCOC₆H₅ 496 N(CH₃)₂ N(CH₃)₂ OCH₂CH₃ H(l = O) OCOC₆H₅ 497 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₂CH₃ H(l = O) OCOC₆H₅ 498 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₂CH₃ H(l = O) OCOC₆H₅ 499 O—(CH₂CH₂)—O OCH₂CH₃ H(l = O) OCOC₆H₅ 500 O—(CH₂CH₂CH₂)—O OCH₂CH₃ H(l = O) OCOC₆H₅ 501 S—(CH₂CH₂)—S OCH₂CH₃ H(l = O) OCOC₆H₅ 502 S—(CH₂CH₂CH₂)—S OCH₂CH₃ H(l = O) OCOC₆H₅ 503 —(CH₂)₄— OCH₂CH₃ H(l = O) OCOC₆H₅ 504 —(CH₂)₅— OCH₂CH₃ H(l = O) OCOC₆H₅ 505 H H SCH₃ H(l = O) OCOC₆H₅ 506 CH₃ CH₃ SCH₃ H(l = O) OCOC₆H₅ 507 CH₂CH₃ CH₂CH₃ SCH₃ H(l = O) OCOC₆H₅ 508 CH₂CH₂CH₃ CH₂CH₂CH₃ SCH₃ H(l = O) OCOC₆H₅ 509 OCH₃ OCH₃ SCH₃ H(l = O) OCOC₆H₅ 510 OCH₂CH₃ OCH₂CH₃ SCH₃ H(l = O) OCOC₆H₅ 511 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SCH₃ H(l = O) OCOC₆H₅ 512 SCH₃ SCH₃ SCH₃ H(l = O) OCOC₆H₅ 513 SCH₂CH₃ SCH₂CH₃ SCH₃ H(l = O) OCOC₆H₅ 514 N(CH₃)₂ N(CH₃)₂ SCH₃ H(l = O) OCOC₆H₅ 515 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SCH₃ H(l = O) OCOC₆H₅ 516 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SCH₃ H(l = O) OCOC₆H₅ 517 O—(CH₂CH₂)—O SCH₃ H(l = O) OCOC₆H₅ 518 O—(CH₂CH₂CH₂)—O SCH₃ H(l = O) OCOC₆H₅ 519 S—(CH₂CH₂)—S SCH₃ H(l = O) OCOC₆H₅ 520 —(CH₂)₄— SCH₃ H(l = O) OCOC₆H₅ 521 —(CH₂)₅— SCH₃ H(l = O) OCOC₆H₅ 522 S—(CH₂CH₂CH₂)—S SCH₃ H(l = O) OCOC₆H₅ 523 —(CH₂)₄— SCH₃ H(l = O) OCOC₆H₅ 524 —(CH₂)₅— SCH₃ H(l = O) OCOC₆H₅ 525 H H SO₂CH₃ H(l = O) OCOC₆H₅ 526 CH₃ CH₃ SO₂CH₃ H(l = O) OCOC₆H₅ 527 CH₂CH₃ CH₂CH₃ SO₂CH₃ H(l = O) OCOC₆H₅ 528 CH₂CH₂CH₃ CH₂CH₂CH₃ SO₂CH₃ H(l = O) OCOC₆H₅ 529 OCH₃ OCH₃ SO₂CH₃ H(l = O) OCOC₆H₅ 530 OCH₂CH₃ OCH₂CH₃ SO₂CH₃ H(l = O) OCOC₆H₅ 531 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SO₂CH₃ H(l = O) OCOC₆H₅ 532 SCH₃ SCH₃ SO₂CH₃ H(l = O) OCOC₆H₅ 533 SCH₂CH₃ SCH₂CH₃ SO₂CH₃ H(l = O) OCOC₆H₅ 534 N(CH₃)₂ N(CH₃)₂ SO₂CH₃ H(l = O) OCOC₆H₅ 535 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SO₂CH₃ H(l = O) OCOC₆H₅ 536 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SO₂CH₃ H(l = O) OCOC₆H₅ 537 O—(CH₂CH₂)—O SO₂CH₃ H(l = O) OCOC₆H₅ 538 O—(CH₂CH₂CH₂)—O SO₂CH₃ H(l = O) OCOC₆H₅ 539 S—(CH₂CH₂)—S SO₂CH₃ H(l = O) OCOC₆H₅ 540 S—(CH₂CH₂CH₂)—S SO₂CH₃ H(l = O) OCOC₆H₅ 541 —(CH₂)₄— SO₂CH₃ H(l = O) OCOC₆H₅ 542 —(CH₂)₅— SO₂CH₃ H(l = O) OCOC₆H₅ 543 H H PO(OCH₃)₂ H(l = O) OCOC₆H₅ 544 CH₃ CH₃ PO(OCH₃)₂ H(l = O) OCOC₆H₅ 545 CH₂CH₃ CH₂CH₃ PO(OCH₃)₂ H(l = O) OCOC₆H₅ 546 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₃)₂ H(l = O) OCOC₆H₅ 547 OCH₃ OCH₃ PO(OCH₃)₂ H(l = O) OCOC₆H₅ 548 OCH₂CH₃ OCH₂CH₃ PO(OCH₃)₂ H(l = O) OCOC₆H₅ 549 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₃)₂ H(l = O) OCOC₆H₅ 550 SCH₃ SCH₃ PO(OCH₃)₂ H(l = O) OCOC₆H₅ 551 SCH₂CH₃ SCH₂CH₃ PO(OCH₃)₂ H(l = O) OCOC₆H₅ 552 N(CH₃)₂ N(CH₃)₂ PO(OCH₃)₂ H(l = O) OCOC₆H₅ 553 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₃)₂ H(l = O) OCOC₆H₅ 554 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₃)₂ H(l = O) OCOC₆H₅ 555 O—(CH₂CH₂)—O PO(OCH₃)₂ H(l = O) OCOC₆H₅ 556 O—(CH₂CH₂CH₂)—O PO(OCH₃)₂ H(l = O) OCOC₆H₅ 557 S—(CH₂CH₂)—S PO(OCH₃)₂ H(l = O) OCOC₆H₅ 558 S—(CH₂CH₂CH₂)—S PO(OCH₃)₂ H(l = O) OCOC₆H₅ 559 —(CH₂)₄— PO(OCH₃)₂ H(l = O) OCOC₆H₅ 560 —(CH₂)₅— PO(OCH₃)₂ H(l = O) OCOC₆H₅ 561 H H PO(OCH₂CH₃)₂ H(l = O) OCOC₆H₅ 562 CH₃ CH₃ PO(OCH₂CH₃)₂ H(l = O) OCOC₆H₅ 563 CH₂CH₃ CH₂CH₃ PO(OCH₂CH₃)₂ H(l = O) OCOC₆H₅ 564 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₂CH₃)₂ H(l = O) OCOC₆H₅ 565 OCH₃ OCH₃ PO(OCH₂CH₃)₂ H(l = O) OCOC₆H₅ 566 OCH₂CH₃ OCH₂CH₃ PO(OCH₂CH₃)₂ H(l = O) OCOC₆H₅ 567 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₂CH₃)₂ H(l = O) OCOC₆H₅ 568 SCH₃ SCH₃ PO(OCH₂CH₃)₂ H(l = O) OCOC₆H₅ 569 SCH₂CH₃ SCH₂CH₃ PO(OCH₂CH₃)₂ H(l = O) OCOC₆H₅ 570 N(CH₃)₂ N(CH₃)₂ PO(OCH₂CH₃)₂ H(l = O) OCOC₆H₅ 571 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₂CH₃)₂ H(l = O) OCOC₆H₅ 572 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₂CH₃)₂ H(l = O) OCOC₆H₅ 573 O—(CH₂CH₂)—O PO(OCH₂CH₃)₂ H(l = O) OCOC₆H₅ 574 O—(CH₂CH₂CH₂)—O PO(OCH₂CH₃)₂ H(l = O) OCOC₆H₅ 575 S—(CH₂CH₂)—S PO(OCH₂CH₃)₂ H(l = O) OCOC₆H₅ 576 S—(CH₂CH₂CH₂)—S PO(OCH₂CH₃)₂ H(l = O) OCOC₆H₅ 577 —(CH₂)₄— PO(OCH₂CH₃)₂ H(l = O) OCOC₆H₅ 578 —(CH₂)₅— PO(OCH₂CH₃)₂ H(l = O) OCOC₆H₅ 579 H H PO(CH₃)₂ H(l = O) OCOC₆H₅ 580 CH₃ CH₃ PO(CH₃)₂ H(l = O) OCOC₆H₅ 581 CH₂CH₃ CH₂CH₃ PO(CH₃)₂ H(l = O) OCOC₆H₅ 582 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₃)₂ H(l = O) OCOC₆H₅ 583 OCH₃ OCH₃ PO(CH₃)₂ H(l = O) OCOC₆H₅ 584 OCH₂CH₃ OCH₂CH₃ PO(CH₃)₂ H(l = O) OCOC₆H₅ 585 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₃)₂ H(l = O) OCOC₆H₅ 586 SCH₃ SCH₃ PO(CH₃)₂ H(l = O) OCOC₆H₅ 587 SCH₂CH₃ SCH₂CH₃ PO(CH₃)₂ H(l = O) OCOC₆H₅ 588 N(CH₃)₂ N(CH₃)₂ PO(CH₃)₂ H(l = O) OCOC₆H₅ 589 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₃)₂ H(l = O) OCOC₆H₅ 590 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₃)₂ H(l = O) OCOC₆H₅ 591 O—(CH₂CH₂)—O PO(CH₃)₂ H(l = O) OCOC₆H₅ 592 O—(CH₂CH₂CH₂)—O PO(CH₃)₂ H(l = O) OCOC₆H₅ 593 S—(CH₂CH₂)—S PO(CH₃)₂ H(l = O) OCOC₆H₅ 594 S—(CH₂CH₂CH₂)—S PO(CH₃)₂ H(l = O) OCOC₆H₅ 595 —(CH₂)₄— PO(CH₃)₂ H(l = O) OCOC₆H₅ 596 —(CH₂)₅— PO(CH₃)₂ H(l = O) OCOC₆H₅ 597 H H PO(CH₂CH₃)₂ H(l = O) OCOC₆H₅ 598 CH₃ CH₃ PO(CH₂CH₃)₂ H(l = O) OCOC₆H₅ 599 CH₂CH₃ CH₂CH₃ PO(CH₂CH₃)₂ H(l = O) OCOC₆H₅ 600 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₂CH₃)₂ H(l = O) OCOC₆H₅ 601 OCH₃ OCH₃ PO(CH₂CH₃)₂ H(l = O) OCOC₆H₅ 602 OCH₂CH₃ OCH₂CH₃ PO(CH₂CH₃)₂ H(l = O) OCOC₆H₅ 603 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₂CH₃)₂ H(l = O) OCOC₆H₅ 604 SCH₃ SCH₃ PO(CH₂CH₃)₂ H(l = O) OCOC₆H₅ 605 SCH₂CH₃ SCH₂CH₃ PO(CH₂CH₃)₂ H(l = O) OCOC₆H₅ 606 N(CH₃)₂ N(CH₃)₂ PO(CH₂CH₃)₂ H(l = O) OCOC₆H₅ 607 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₂CH₃)₂ H(l = O) OCOC₆H₅ 608 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₂CH₃)₂ H(l = O) OCOC₆H₅ 609 O—(CH₂CH₂)—O PO(CH₂CH₃)₂ H(l = O) OCOC₆H₅ 610 O—(CH₂CH₂CH₂)—O PO(CH₂CH₃)₂ H(l = O) OCOC₆H₅ 611 S—(CH₂CH₂)—S PO(CH₂CH₃)₂ H(l = O) OCOC₆H₅ 612 S—(CH₂CH₂CH₂)—S PO(CH₂CH₃)₂ H(l = O) OCOC₆H₅ 613 —(CH₂)₄— PO(CH₂CH₃)₂ H(l = O) OCOC₆H₅ 614 —(CH₂)₅— PO(CH₂CH₃)₂ H(l = O) OCOC₆H₅ 615 H H H H(l = O) SCH₃ 616 CH₃ CH₃ H H(l = O) SCH₃ 617 CH₂CH₃ CH₂CH₃ H H(l = O) SCH₃ 618 CH₂CH₂CH₃ CH₂CH₂CH₃ H H(l = O) SCH₃ 619 OCH₃ OCH₃ H H(l = O) SCH₃ 620 OCH₂CH₃ OCH₂CH₃ H H(l = O) SCH₃ 621 OCH₂CH₂CH₃ OCH₂CH₂CH₃ H H(l = O) SCH₃ 622 SCH₃ SCH₃ H H(l = O) SCH₃ 623 SCH₂CH₃ SCH₂CH₃ H H(l = O) SCH₃ 624 N(CH₃)₂ N(CH₃)₂ H H(l = O) SCH₃ 625 N(CH₂CH₃)₂ N(CH₂CH₃)₂ H H(l = O) SCH₃ 626 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) H H(l = O) SCH₃ 627 O—(CH₂CH₂)—O H H(l = O) SCH₃ 628 O—(CH₂CH₂CH₂)—O H H(l = O) SCH₃ 629 S—(CH₂CH₂)—S H H(l = O) SCH₃ 630 S—(CH₂CH₂CH₂)—S H H(l = O) SCH₃ 631 —(CH₂)₄— H H(l = O) SCH₃ 632 —(CH₂)₅— H H(l = O) SCH₃ 633 H H NO₂ H(l = O) SCH₃ 634 CH₃ CH₃ NO₂ H(l = O) SCH₃ 635 CH₂CH₃ CH₂CH₃ NO₂ H(l = O) SCH₃ 636 CH₂CH₂CH₃ CH₂CH₂CH₃ NO₂ H(l = O) SCH₃ 637 OCH₃ OCH₃ NO₂ H(l = O) SCH₃ 638 OCH₂CH₃ OCH₂CH₃ NO₂ H(l = O) SCH₃ 639 OCH₂CH₂CH₃ OCH₂CH₂CH₃ NO₂ H(l = O) SCH₃ 640 SCH₃ SCH₃ NO₂ H(l = O) SCH₃ 641 SCH₂CH₃ SCH₂CH₃ NO₂ H(l = O) SCH₃ 642 N(CH₃)₂ N(CH₃)₂ NO₂ H(l = O) SCH₃ 643 N(CH₂CH₃)₂ N(CH₂CH₃)₂ NO₂ H(l = O) SCH₃ 644 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) NO₂ H(l = O) SCH₃ 645 O—(CH₂CH₂)—O NO₂ H(l = O) SCH₃ 646 O—(CH₂CH₂CH₂)—O NO₂ H(l = O) SCH₃ 647 S—(CH₂CH₂)—S NO₂ H(l = O) SCH₃ 648 S—(CH₂CH₂CH₂)—S NO₂ H(l = O) SCH₃ 649 —(CH₂)₄— NO₂ H(l = O) SCH₃ 650 —(CH₂)₅— NO₂ H(l = O) SCH₃ 651 H H CN H(l = O) SCH₃ 652 CH₃ CH₃ CN H(l = O) SCH₃ 653 CH₂CH₃ CH₂CH₃ CN H(l = O) SCH₃ 654 CH₂CH₂CH₃ CH₂CH₂CH₃ CN H(l = O) SCH₃ 655 OCH₃ OCH₃ CN H(l = O) SCH₃ 656 OCH₂CH₃ OCH₂CH₃ CN H(l = O) SCH₃ 657 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CN H(l = O) SCH₃ 658 SCH₃ SCH₃ CN H(l = O) SCH₃ 659 SCH₂CH₃ SCH₂CH₃ CN H(l = O) SCH₃ 660 N(CH₃)₂ N(CH₃)₂ CN H(l = O) SCH₃ 661 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CN H(l = O) SCH₃ 662 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CN H(l = O) SCH₃ 663 O—(CH₂CH₂)—O CN H(l = O) SCH₃ 664 O—(CH₂CH₂CH₂)—O CN H(l = O) SCH₃ 665 S—(CH₂CH₂)—S CN H(l = O) SCH₃ 666 S—(CH₂CH₂CH₂)—S CN H(l = O) SCH₃ 667 —(CH₂)₄— CN H(l = O) SCH₃ 668 —(CH₂)₅— CN H(l = O) SCH₃ 669 H H F H(l = O) SCH₃ 670 CH₃ CH₃ F H(l = O) SCH₃ 671 CH₂CH₃ CH₂CH₃ F H(l = O) SCH₃ 672 CH₂CH₂CH₃ CH₂CH₂CH₃ F H(l = O) SCH₃ 673 OCH₃ OCH₃ F H(l = O) SCH₃ 674 OCH₂CH₃ OCH₂CH₃ F H(l = O) SCH₃ 675 OCH₂CH₂CH₃ OCH₂CH₂CH₃ F H(l = O) SCH₃ 676 SCH₃ SCH₃ F H(l = O) SCH₃ 677 SCH₂CH₃ SCH₂CH₃ F H(l = O) SCH₃ 678 N(CH₃)₂ N(CH₃)₂ F H(l = O) SCH₃ 679 N(CH₂CH₃)₂ N(CH₂CH₃)₂ F H(l = O) SCH₃ 680 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) F H(l = O) SCH₃ 681 O—(CH₂CH₂)—O F H(l = O) SCH₃ 682 O—(CH₂CH₂CH₂)—O F H(l = O) SCH₃ 683 S—(CH₂CH₂)—S F H(l = O) SCH₃ 684 S—(CH₂CH₂CH₂)—S F H(l = O) SCH₃ 685 —(CH₂)₄— F H(l = O) SCH₃ 686 —(CH₂)₅— F H(l = O) SCH₃ 687 H H Cl H(l = O) SCH₃ 688 CH₃ CH₃ Cl H(l = O) SCH₃ 689 CH₂CH₃ CH₂CH₃ Cl H(l = O) SCH₃ 690 CH₂CH₂CH₃ CH₂CH₂CH₃ Cl H(l = O) SCH₃ 691 OCH₃ OCH₃ Cl H(l = O) SCH₃ 692 OCH₂CH₃ OCH₂CH₃ Cl H(l = O) SCH₃ 693 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Cl H(l = O) SCH₃ 694 SCH₃ SCH₃ Cl H(l = O) SCH₃ 695 SCH₂CH₃ SCH₂CH₃ Cl H(l = O) SCH₃ 696 N(CH₃)₂ N(CH₃)₂ Cl H(l = O) SCH₃ 697 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Cl H(l = O) SCH₃ 698 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Cl H(l = O) SCH₃ 699 O—(CH₂CH₂)—O Cl H(l = O) SCH₃ 700 O—(CH₂CH₂CH₂)—O Cl H(l = O) SCH₃ 701 S—(CH₂CH₂)—S Cl H(l = O) SCH₃ 702 S—(CH₂CH₂CH₂)—S Cl H(l = O) SCH₃ 703 —(CH₂)₄— Cl H(l = O) SCH₃ 704 —(CH₂)₅— Cl H(l = O) SCH₃ 705 H H Br H(l = O) SCH₃ 706 CH₃ CH₃ Br H(l = O) SCH₃ 707 CH₂CH₃ CH₂CH₃ Br H(l = O) SCH₃ 708 CH₂CH₂CH₃ CH₂CH₂CH₃ Br H(l = O) SCH₃ 709 OCH₃ OCH₃ Br H(l = O) SCH₃ 710 OCH₂CH₃ OCH₂CH₃ Br H(l = O) SCH₃ 711 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Br H(l = O) SCH₃ 712 SCH₃ SCH₃ Br H(l = O) SCH₃ 713 SCH₂CH₃ SCH₂CH₃ Br H(l = O) SCH₃ 714 N(CH₃)₂ N(CH₃)₂ Br H(l = O) SCH₃ 715 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Br H(l = O) SCH₃ 716 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Br H(l = O) SCH₃ 717 O—(CH₂CH₂)—O Br H(l = O) SCH₃ 718 O—(CH₂CH₂CH₂)—O Br H(l = O) SCH₃ 719 S—(CH₂CH₂)—S Br H(l = O) SCH₃ 720 S—(CH₂CH₂CH₂)—S Br H(l = O) SCH₃ 721 —(CH₂)₄— Br H(l = O) SCH₃ 722 —(CH₂)₅— Br H(l = O) SCH₃ 723 H H CH₃ H(l = O) SCH₃ 724 CH₃ CH₃ CH₃ H(l = O) SCH₃ 725 CH₂CH₃ CH₂CH₃ CH₃ H(l = O) SCH₃ 726 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₃ H(l = O) SCH₃ 727 OCH₃ OCH₃ CH₃ H(l = O) SCH₃ 728 OCH₂CH₃ OCH₂CH₃ CH₃ H(l = O) SCH₃ 729 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₃ H(l = O) SCH₃ 730 SCH₃ SCH₃ CH₃ H(l = O) SCH₃ 731 SCH₂CH₃ SCH₂CH₃ CH₃ H(l = O) SCH₃ 732 N(CH₃)₂ N(CH₃)₂ CH₃ H(l = O) SCH₃ 733 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₃ H(l = O) SCH₃ 734 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₃ H(l = O) SCH₃ 735 O—(CH₂CH₂)—O CH₃ H(l = O) SCH₃ 736 O—(CH₂CH₂CH₂)—O CH₃ H(l = O) SCH₃ 737 S—(CH₂CH₂)—S CH₃ H(l = O) SCH₃ 738 S—(CH₂CH₂CH₂)—S CH₃ H(l = O) SCH₃ 739 —(CH₂)₄— CH₃ H(l = O) SCH₃ 740 —(CH₂)₅— CH₃ H(l = O) SCH₃ 741 H H CH₂CH₃ H(l = O) SCH₃ 742 CH₃ CH₃ CH₂CH₃ H(l = O) SCH₃ 743 CH₂CH₃ CH₂CH₃ CH₂CH₃ H(l = O) SCH₃ 744 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₂CH₃ H(l = O) SCH₃ 745 OCH₃ OCH₃ CH₂CH₃ H(l = O) SCH₃ 746 OCH₂CH₃ OCH₂CH₃ CH₂CH₃ H(l = O) SCH₃ 747 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₂CH₃ H(l = O) SCH₃ 748 SCH₃ SCH₃ CH₂CH₃ H(l = O) SCH₃ 749 SCH₂CH₃ SCH₂CH₃ CH₂CH₃ H(l = O) SCH₃ 750 N(CH₃)₂ N(CH₃)₂ CH₂CH₃ H(l = O) SCH₃ 751 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₂CH₃ H(l = O) SCH₃ 752 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₂CH₃ H(l = O) SCH₃ 753 O—(CH₂CH₂)—O CH₂CH₃ H(l = O) SCH₃ 754 O—(CH₂CH₂CH₂)—O CH₂CH₃ H(l = O) SCH₃ 755 S—(CH₂CH₂)—S CH₂CH₃ H(l = O) SCH₃ 756 S—(CH₂CH₂CH₂)—S CH₂CH₃ H(l = O) SCH₃ 757 —(CH₂)₄— CH₂CH₃ H(l = O) SCH₃ 758 —(CH₂)₅— CH₂CH₃ H(l = O) SCH₃ 759 H H CF₃ H(l = O) SCH₃ 760 CH₃ CH₃ CF₃ H(l = O) SCH₃ 761 CH₂CH₃ CH₂CH₃ CF₃ H(l = O) SCH₃ 762 CH₂CH₂CH₃ CH₂CH₂CH₃ CF₃ H(l = O) SCH₃ 763 OCH₃ OCH₃ CF₃ H(l = O) SCH₃ 764 OCH₂CH₃ OCH₂CH₃ CF₃ H(l = O) SCH₃ 765 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CF₃ H(l = O) SCH₃ 766 SCH₃ SCH₃ CF₃ H(l = O) SCH₃ 767 SCH₂CH₃ SCH₂CH₃ CF₃ H(l = O) SCH₃ 768 N(CH₃)₂ N(CH₃)₂ CF₃ H(l = O) SCH₃ 769 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CF₃ H(l = O) SCH₃ 770 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CF₃ H(l = O) SCH₃ 771 O—(CH₂CH₂)—O CF₃ H(l = O) SCH₃ 772 O—(CH₂CH₂CH₂)—O CF₃ H(l = O) SCH₃ 773 S—(CH₂CH₂)—S CF₃ H(l = O) SCH₃ 774 S—(CH₂CH₂CH₂)—S CF₃ H(l = O) SCH₃ 775 —(CH₂)₄— CF₃ H(l = O) SCH₃ 776 —(CH₂)₅— CF₃ H(l = O) SCH₃ 777 H H OCH₃ H(l = O) SCH₃ 778 CH₃ CH₃ OCH₃ H(l = O) SCH₃ 779 CH₂CH₃ CH₂CH₃ OCH₃ H(l = O) SCH₃ 780 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₃ H(l = O) SCH₃ 781 OCH₃ OCH₃ OCH₃ H(l = O) SCH₃ 782 OCH₂CH₃ OCH₂CH₃ OCH₃ H(l = O) SCH₃ 783 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₃ H(l = O) SCH₃ 784 SCH₃ SCH₃ OCH₃ H(l = O) SCH₃ 785 SCH₂CH₃ SCH₂CH₃ OCH₃ H(l = O) SCH₃ 786 N(CH₃)₂ N(CH₃)₂ OCH₃ H(l = O) SCH₃ 787 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₃ H(l = O) SCH₃ 788 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₃ H(l = O) SCH₃ 789 O—(CH₂CH₂)—O OCH₃ H(l = O) SCH₃ 790 O—(CH₂CH₂CH₂)—O OCH₃ H(l = O) SCH₃ 791 S—(CH₂CH₂)—S OCH₃ H(l = O) SCH₃ 792 S—(CH₂CH₂CH₂)—S OCH₃ H(l = O) SCH₃ 793 —(CH₂)₄— OCH₃ H(l = O) SCH₃ 794 —(CH₂)₅— OCH₃ H(l = O) SCH₃ 795 H H OCH₂CH₃ H(l = O) SCH₃ 796 CH₃ CH₃ OCH₂CH₃ H(l = O) SCH₃ 797 CH₂CH₃ CH₂CH₃ OCH₂CH₃ H(l = O) SCH₃ 798 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₂CH₃ H(l = O) SCH₃ 799 OCH₃ OCH₃ OCH₂CH₃ H(l = O) SCH₃ 800 OCH₂CH₃ OCH₂CH₃ OCH₂CH₃ H(l = O) SCH₃ 801 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₂CH₃ H(l = O) SCH₃ 802 SCH₃ SCH₃ OCH₂CH₃ H(l = O) SCH₃ 803 SCH₂CH₃ SCH₂CH₃ OCH₂CH₃ H(l = O) SCH₃ 804 N(CH₃)₂ N(CH₃)₂ OCH₂CH₃ H(l = O) SCH₃ 805 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₂CH₃ H(l = O) SCH₃ 806 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₂CH₃ H(l = O) SCH₃ 807 O—(CH₂CH₂)—O OCH₂CH₃ H(l = O) SCH₃ 808 O—(CH₂CH₂CH₂)—O OCH₂CH₃ H(l = O) SCH₃ 809 S—(CH₂CH₂)—S OCH₂CH₃ H(l = O) SCH₃ 810 S—(CH₂CH₂CH₂)—S OCH₂CH₃ H(l = O) SCH₃ 811 —(CH₂)₄— OCH₂CH₃ H(l = O) SCH₃ 812 —(CH₂)₅— OCH₂CH₃ H(l = O) SCH₃ 813 H H SCH₃ H(l = O) SCH₃ 814 CH₃ CH₃ SCH₃ H(l = O) SCH₃ 815 CH₂CH₃ CH₂CH₃ SCH₃ H(l = O) SCH₃ 816 CH₂CH₂CH₃ CH₂CH₂CH₃ SCH₃ H(l = O) SCH₃ 817 OCH₃ OCH₃ SCH₃ H(l = O) SCH₃ 818 OCH₂CH₃ OCH₂CH₃ SCH₃ H(l = O) SCH₃ 819 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SCH₃ H(l = O) SCH₃ 820 SCH₃ SCH₃ SCH₃ H(l = O) SCH₃ 821 SCH₂CH₃ SCH₂CH₃ SCH₃ H(l = O) SCH₃ 822 N(CH₃)₂ N(CH₃)₂ SCH₃ H(l = O) SCH₃ 823 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SCH₃ H(l = O) SCH₃ 824 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SCH₃ H(l = O) SCH₃ 825 O—(CH₂CH₂)—O SCH₃ H(l = O) SCH₃ 826 O—(CH₂CH₂CH₂)—O SCH₃ H(l = O) SCH₃ 827 S—(CH₂CH₂)—S SCH₃ H(l = O) SCH₃ 828 S—(CH₂CH₂CH₂)—S SCH₃ H(l = O) SCH₃ 829 —(CH₂)₄— SCH₃ H(l = O) SCH₃ 830 —(CH₂)₅— SCH₃ H(l = O) SCH₃ 831 H H SO₂CH₃ H(l = O) SCH₃ 832 CH₃ CH₃ SO₂CH₃ H(l = O) SCH₃ 833 CH₂CH₃ CH₂CH₃ SO₂CH₃ H(l = O) SCH₃ 834 CH₂CH₂CH₃ CH₂CH₂CH₃ SO₂CH₃ H(l = O) SCH₃ 835 OCH₃ OCH₃ SO₂CH₃ H(l = O) SCH₃ 836 OCH₂CH₃ OCH₂CH₃ SO₂CH₃ H(l = O) SCH₃ 837 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SO₂CH₃ H(l = O) SCH₃ 838 SCH₃ SCH₃ SO₂CH₃ H(l = O) SCH₃ 839 SCH₂CH₃ SCH₂CH₃ SO₂CH₃ H(l = O) SCH₃ 840 N(CH₃)₂ N(CH₃)₂ SO₂CH₃ H(l = O) SCH₃ 841 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SO₂CH₃ H(l = O) SCH₃ 842 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SO₂CH₃ H(l = O) SCH₃ 843 O—(CH₂CH₂)—O SO₂CH₃ H(l = O) SCH₃ 844 O—(CH₂CH₂CH₂)—O SO₂CH₃ H(l = O) SCH₃ 845 S—(CH₂CH₂)—S SO₂CH₃ H(l = O) SCH₃ 846 S—(CH₂CH₂CH₂)—S SO₂CH₃ H(l = O) SCH₃ 847 —(CH₂)₄— SO₂CH₃ H(l = O) SCH₃ 848 —(CH₂)₅— SO₂CH₃ H(l = O) SCH₃ 849 H H PO(OCH₃)₂ H(l = O) SCH₃ 850 CH₃ CH₃ PO(OCH₃)₂ H(l = O) SCH₃ 851 CH₂CH₃ CH₂CH₃ PO(OCH₃)₂ H(l = O) SCH₃ 852 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₃)₂ H(l = O) SCH₃ 853 OCH₃ OCH₃ PO(OCH₃)₂ H(l = O) SCH₃ 854 OCH₂CH₃ OCH₂CH₃ PO(OCH₃)₂ H(l = O) SCH₃ 855 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₃)₂ H(l = O) SCH₃ 856 SCH₃ SCH₃ PO(OCH₃)₂ H(l = O) SCH₃ 857 SCH₂CH₃ SCH₂CH₃ PO(OCH₃)₂ H(l = O) SCH₃ 858 N(CH₃)₂ N(CH₃)₂ PO(OCH₃)₂ H(l = O) SCH₃ 859 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₃)₂ H(l = O) SCH₃ 860 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₃)₂ H(l = O) SCH₃ 861 O—(CH₂CH₂)—O PO(OCH₃)₂ H(l = O) SCH₃ 862 O—(CH₂CH₂CH₂)—O PO(OCH₃)₂ H(l = O) SCH₃ 863 S—(CH₂CH₂)—S PO(OCH₃)₂ H(l = O) SCH₃ 864 S—(CH₂CH₂CH₂)—S PO(OCH₃)₂ H(l = O) SCH₃ 865 —(CH₂)₄— PO(OCH₃)₂ H(l = O) SCH₃ 866 —(CH₂)₅— PO(OCH₃)₂ H(l = O) SCH₃ 867 H H PO(OCH₂CH₃)₂ H(l = O) SCH₃ 868 CH₃ CH₃ PO(OCH₂CH₃)₂ H(l = O) SCH₃ 869 CH₂CH₃ CH₂CH₃ PO(OCH₂CH₃)₂ H(l = O) SCH₃ 870 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₂CH₃)₂ H(l = O) SCH₃ 871 OCH₃ OCH₃ PO(OCH₂CH₃)₂ H(l = O) SCH₃ 872 OCH₂CH₃ OCH₂CH₃ PO(OCH₂CH₃)₂ H(l = O) SCH₃ 873 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₂CH₃)₂ H(l = O) SCH₃ 874 SCH₃ SCH₃ PO(OCH₂CH₃)₂ H(l = O) SCH₃ 875 SCH₂CH₃ SCH₂CH₃ PO(OCH₂CH₃)₂ H(l = O) SCH₃ 876 N(CH₃)₂ N(CH₃)₂ PO(OCH₂CH₃)₂ H(l = O) SCH₃ 877 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₂CH₃)₂ H(l = O) SCH₃ 878 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₂CH₃)₂ H(l = O) SCH₃ 879 O—(CH₂CH₂)—O PO(OCH₂CH₃)₂ H(l = O) SCH₃ 880 O—(CH₂CH₂CH₂)—O PO(OCH₂CH₃)₂ H(l = O) SCH₃ 881 S—(CH₂CH₂)—S PO(OCH₂CH₃)₂ H(l = O) SCH₃ 882 S—(CH₂CH₂CH₂)—S PO(OCH₂CH₃)₂ H(l = O) SCH₃ 883 —(CH₂)₄— PO(OCH₂CH₃)₂ H(l = O) SCH₃ 884 —(CH₂)₅— PO(OCH₂CH₃)₂ H(l = O) SCH₃ 885 H H PO(CH₃)₂ H(l = O) SCH₃ 886 CH₃ CH₃ PO(CH₃)₂ H(l = O) SCH₃ 887 CH₂CH₃ CH₂CH₃ PO(CH₃)₂ H(l = O) SCH₃ 888 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₃)₂ H(l = O) SCH₃ 889 OCH₃ OCH₃ PO(CH₃)₂ H(l = O) SCH₃ 890 OCH₂CH₃ OCH₂CH₃ PO(CH₃)₂ H(l = O) SCH₃ 891 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₃)₂ H(l = O) SCH₃ 892 SCH₃ SCH₃ PO(CH₃)₂ H(l = O) SCH₃ 893 SCH₂CH₃ SCH₂CH₃ PO(CH₃)₂ H(l = O) SCH₃ 894 N(CH₃)₂ N(CH₃)₂ PO(CH₃)₂ H(l = O) SCH₃ 895 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₃)₂ H(l = O) SCH₃ 896 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₃)₂ H(l = O) SCH₃ 897 O—(CH₂CH₂)—O PO(CH₃)₂ H(l = O) SCH₃ 898 O—(CH₂CH₂CH₂)—O PO(CH₃)₂ H(l = O) SCH₃ 899 S—(CH₂CH₂)—S PO(CH₃)₂ H(l = O) SCH₃ 900 S—(CH₂CH₂CH₂)—S PO(CH₃)₂ H(l = O) SCH₃ 901 —(CH₂)₄— PO(CH₃)₂ H(l = O) SCH₃ 902 —(CH₂)₅— PO(CH₃)₂ H(l = O) SCH₃ 903 H H PO(CH₂CH₃)₂ H(l = O) SCH₃ 904 CH₃ CH₃ PO(CH₂CH₃)₂ H(l = O) SCH₃ 905 CH₂CH₃ CH₂CH₃ PO(CH₂CH₃)₂ H(l = O) SCH₃ 906 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₂CH₃)₂ H(l = O) SCH₃ 907 OCH₃ OCH₃ PO(CH₂CH₃)₂ H(l = O) SCH₃ 908 OCH₂CH₃ OCH₂CH₃ PO(CH₂CH₃)₂ H(l = O) SCH₃ 909 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₂CH₃)₂ H(l = O) SCH₃ 910 SCH₃ SCH₃ PO(CH₂CH₃)₂ H(l = O) SCH₃ 911 SCH₂CH₃ SCH₂CH₃ PO(CH₂CH₃)₂ H(l = O) SCH₃ 912 N(CH₃)₂ N(CH₃)₂ PO(CH₂CH₃)₂ H(l = O) SCH₃ 913 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₂CH₃)₂ H(l = O) SCH₃ 914 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₂CH₃)₂ H(l = O) SCH₃ 915 O—(CH₂CH₂)—O PO(CH₂CH₃)₂ H(l = O) SCH₃ 916 O—(CH₂CH₂CH₂)—O PO(CH₂CH₃)₂ H(l = O) SCH₃ 917 S—(CH₂CH₂)—S PO(CH₂CH₃)₂ H(l = O) SCH₃ 918 S—(CH₂CH₂CH₂)—S PO(CH₂CH₃)₂ H(l = O) SCH₃ 919 —(CH₂)₄— PO(CH₂CH₃)₂ H(l = O) SCH₃ 920 —(CH₂)₅— PO(CH₂CH₃)₂ H(l = O) SCH₃ 921 H H H H(l = O) SC₆H₅ 922 CH₃ CH₃ H H(l = O) SC₆H₅ 923 CH₂CH₃ CH₂CH₃ H H(l = O) SC₆H₅ 924 CH₂CH₂CH₃ CH₂CH₂CH₃ H H(l = O) SC₆H₅ 925 OCH₃ OCH₃ H H(l = O) SC₆H₅ 926 OCH₂CH₃ OCH₂CH₃ H H(l = O) SC₆H₅ 927 OCH₂CH₂CH₃ OCH₂CH₂CH₃ H H(l = O) SC₆H₅ 928 SCH₃ SCH₃ H H(l = O) SC₆H₅ 929 SCH₂CH₃ SCH₂CH₃ H H(l = O) SC₆H₅ 930 N(CH₃)₂ N(CH₃)₂ H H(l = O) SC₆H₅ 931 N(CH₂CH₃)₂ N(CH₂CH₃)₂ H H(l = O) SC₆H₅ 932 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) H H(l = O) SC₆H₅ 933 O—(CH₂CH₂)—O H H(l = O) SC₆H₅ 934 O—(CH₂CH₂CH₂)—O H H(l = O) SC₆H₅ 935 S—(CH₂CH₂)—S H H(l = O) SC₆H₅ 936 S—(CH₂CH₂CH₂)—S H H(l = O) SC₆H₅ 937 —(CH₂)₄— H H(l = O) SC₆H₅ 938 —(CH₂)₅— H H(l = O) SC₆H₅ 939 H H NO₂ H(l = O) SC₆H₅ 940 CH₃ CH₃ NO₂ H(l = O) SC₆H₅ 941 CH₂CH₃ CH₂CH₃ NO₂ H(l = O) SC₆H₅ 942 CH₂CH₂CH₃ CH₂CH₂CH₃ NO₂ H(l = O) SC₆H₅ 943 OCH₃ OCH₃ NO₂ H(l = O) SC₆H₅ 944 OCH₂CH₃ OCH₂CH₃ NO₂ H(l = O) SC₆H₅ 945 OCH₂CH₂CH₃ OCH₂CH₂CH₃ NO₂ H(l = O) SC₆H₅ 946 SCH₃ SCH₃ NO₂ H(l = O) SC₆H₅ 947 SCH₂CH₃ SCH₂CH₃ NO₂ H(l = O) SC₆H₅ 948 N(CH₃)₂ N(CH₃)₂ NO₂ H(l = O) SC₆H₅ 949 N(CH₂CH₃)₂ N(CH₂CH₃)₂ NO₂ H(l = O) SC₆H₅ 950 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) NO₂ H(l = O) SC₆H₅ 951 O—(CH₂CH₂)—O NO₂ H(l = O) SC₆H₅ 952 O—(CH₂CH₂CH₂)—O NO₂ H(l = O) SC₆H₅ 953 S—(CH₂CH₂)—S NO₂ H(l = O) SC₆H₅ 954 S—(CH₂CH₂CH₂)—S NO₂ H(l = O) SC₆H₅ 955 —(CH₂)₄— NO₂ H(l = O) SC₆H₅ 956 —(CH₂)₅— NO₂ H(l = O) SC₆H₅ 957 H H CN H(l = O) SC₆H₅ 958 CH₃ CH₃ CN H(l = O) SC₆H₅ 959 CH₂CH₃ CH₂CH₃ CN H(l = O) SC₆H₅ 960 CH₂CH₂CH₃ CH₂CH₂CH₃ CN H(l = O) SC₆H₅ 961 OCH₃ OCH₃ CN H(l = O) SC₆H₅ 962 OCH₂CH₃ OCH₂CH₃ CN H(l = O) SC₆H₅ 963 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CN H(l = O) SC₆H₅ 964 SCH₃ SCH₃ CN H(l = O) SC₆H₅ 965 SCH₂CH₃ SCH₂CH₃ CN H(l = O) SC₆H₅ 966 N(CH₃)₂ N(CH₃)₂ CN H(l = O) SC₆H₅ 967 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CN H(l = O) SC₆H₅ 968 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CN H(l = O) SC₆H₅ 969 O—(CH₂CH₂)—O CN H(l = O) SC₆H₅ 970 O—(CH₂CH₂CH₂)—O CN H(l = O) SC₆H₅ 971 S—(CH₂CH₂)—S CN H(l = O) SC₆H₅ 972 S—(CH₂CH₂CH₂)—S CN H(l = O) SC₆H₅ 973 —(CH₂)₄— CN H(l = O) SC₆H₅ 974 —(CH₂)₅— CN H(l = O) SC₆H₅ 975 H H F H(l = O) SC₆H₅ 976 CH₃ CH₃ F H(l = O) SC₆H₅ 977 CH₂CH₃ CH₂CH₃ F H(l = O) SC₆H₅ 978 CH₂CH₂CH₃ CH₂CH₂CH₃ F H(l = O) SC₆H₅ 979 OCH₃ OCH₃ F H(l = O) SC₆H₅ 980 OCH₂CH₃ OCH₂CH₃ F H(l = O) SC₆H₅ 981 OCH₂CH₂CH₃ OCH₂CH₂CH₃ F H(l = O) SC₆H₅ 982 SCH₃ SCH₃ F H(l = O) SC₆H₅ 983 SCH₂CH₃ SCH₂CH₃ F H(l = O) SC₆H₅ 984 N(CH₃)₂ N(CH₃)₂ F H(l = O) SC₆H₅ 985 N(CH₂CH₃)₂ N(CH₂CH₃)₂ F H(l = O) SC₆H₅ 986 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) F H(l = O) SC₆H₅ 987 O—(CH₂CH₂)—O F H(l = O) SC₆H₅ 988 O—(CH₂CH₂CH₂)—O F H(l = O) SC₆H₅ 989 S—(CH₂CH₂)—S F H(l = O) SC₆H₅ 990 S—(CH₂CH₂CH₂)—S F H(l = O) SC₆H₅ 991 —(CH₂)₄— F H(l = O) SC₆H₅ 992 —(CH₂)₅— F H(l = O) SC₆H₅ 993 H H Cl H(l = O) SC₆H₅ 994 CH₃ CH₃ Cl H(l = O) SC₆H₅ 995 CH₂CH₃ CH₂CH₃ Cl H(l = O) SC₆H₅ 996 CH₂CH₂CH₃ CH₂CH₂CH₃ Cl H(l = O) SC₆H₅ 997 OCH₃ OCH₃ Cl H(l = O) SC₆H₅ 998 OCH₂CH₃ OCH₂CH₃ Cl H(l = O) SC₆H₅ 999 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Cl H(l = O) SC₆H₅ 1000 SCH₃ SCH₃ Cl H(l = O) SC₆H₅ 1001 SCH₂CH₃ SCH₂CH₃ Cl H(l = O) SC₆H₅ 1002 N(CH₃)₂ N(CH₃)₂ Cl H(l = O) SC₆H₅ 1003 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Cl H(l = O) SC₆H₅ 1004 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Cl H(l = O) SC₆H₅ 1005 O—(CH₂CH₂)—O Cl H(l = O) SC₆H₅ 1006 O—(CH₂CH₂CH₂)—O Cl H(l = O) SC₆H₅ 1007 S—(CH₂CH₂)—S Cl H(l = O) SC₆H₅ 1008 S—(CH₂CH₂CH₂)—S Cl H(l = O) SC₆H₅ 1009 —(CH₂)₄— Cl H(l = O) SC₆H₅ 1010 —(CH₂)₅— Cl H(l = O) SC₆H₅ 1011 H H Br H(l = O) SC₆H₅ 1012 CH₃ CH₃ Br H(l = O) SC₆H₅ 1013 CH₂CH₃ CH₂CH₃ Br H(l = O) SC₆H₅ 1014 CH₂CH₂CH₃ CH₂CH₂CH₃ Br H(l = O) SC₆H₅ 1015 OCH₃ OCH₃ Br H(l = O) SC₆H₅ 1016 OCH₂CH₃ OCH₂CH₃ Br H(l = O) SC₆H₅ 1017 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Br H(l = O) SC₆H₅ 1018 SCH₃ SCH₃ Br H(l = O) SC₆H₅ 1019 SCH₂CH₃ SCH₂CH₃ Br H(l = O) SC₆H₅ 1020 N(CH₃)₂ N(CH₃)₂ Br H(l = O) SC₆H₅ 1021 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Br H(l = O) SC₆H₅ 1022 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Br H(l = O) SC₆H₅ 1023 O—(CH₂CH₂)—O Br H(l = O) SC₆H₅ 1024 O—(CH₂CH₂CH₂)—O Br H(l = O) SC₆H₅ 1025 S—(CH₂CH₂)—S Br H(l = O) SC₆H₅ 1026 S—(CH₂CH₂CH₂)—S Br H(l = O) SC₆H₅ 1027 —(CH₂)₄— Br H(l = O) SC₆H₅ 1028 —(CH₂)₅— Br H(l = O) SC₆H₅ 1029 H H CH₃ H(l = O) SC₆H₅ 1030 CH₃ CH₃ CH₃ H(l = O) SC₆H₅ 1031 CH₂CH₃ CH₂CH₃ CH₃ H(l = O) SC₆H₅ 1032 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₃ H(l = O) SC₆H₅ 1033 OCH₃ OCH₃ CH₃ H(l = O) SC₆H₅ 1034 OCH₂CH₃ OCH₂CH₃ CH₃ H(l = O) SC₆H₅ 1035 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₃ H(l = O) SC₆H₅ 1036 SCH₃ SCH₃ CH₃ H(l = O) SC₆H₅ 1037 SCH₂CH₃ SCH₂CH₃ CH₃ H(l = O) SC₆H₅ 1038 N(CH₃)₂ N(CH₃)₂ CH₃ H(l = O) SC₆H₅ 1039 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₃ H(l = O) SC₆H₅ 1040 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₃ H(l = O) SC₆H₅ 1041 O—(CH₂CH₂)—O CH₃ H(l = O) SC₆H₅ 1042 O—(CH₂CH₂CH₂)—O CH₃ H(l = O) SC₆H₅ 1043 S—(CH₂CH₂)—S CH₃ H(l = O) SC₆H₅ 1044 S—(CH₂CH₂CH₂)—S CH₃ H(l = O) SC₆H₅ 1045 —(CH₂)₄— CH₃ H(l = O) SC₆H₅ 1046 —(CH₂)₅— CH₃ H(l = O) SC₆H₅ 1047 H H CH₂CH₃ H(l = O) SC₆H₅ 1048 CH₃ CH₃ CH₂CH₃ H(l = O) SC₆H₅ 1049 CH₂CH₃ CH₂CH₃ CH₂CH₃ H(l = O) SC₆H₅ 1050 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₂CH₃ H(l = O) SC₆H₅ 1051 OCH₃ OCH₃ CH₂CH₃ H(l = O) SC₆H₅ 1052 OCH₂CH₃ OCH₂CH₃ CH₂CH₃ H(l = O) SC₆H₅ 1053 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₂CH₃ H(l = O) SC₆H₅ 1054 SCH₃ SCH₃ CH₂CH₃ H(l = O) SC₆H₅ 1055 SCH₂CH₃ SCH₂CH₃ CH₂CH₃ H(l = O) SC₆H₅ 1056 N(CH₃)₂ N(CH₃)₂ CH₂CH₃ H(l = O) SC₆H₅ 1057 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₂CH₃ H(l = O) SC₆H₅ 1058 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₂CH₃ H(l = O) SC₆H₅ 1059 O—(CH₂CH₂)—O CH₂CH₃ H(l = O) SC₆H₅ 1060 O—(CH₂CH₂CH₂)—O CH₂CH₃ H(l = O) SC₆H₅ 1061 S—(CH₂CH₂)—S CH₂CH₃ H(l = O) SC₆H₅ 1062 S—(CH₂CH₂CH₂)—S CH₂CH₃ H(l = O) SC₆H₅ 1063 —(CH₂)₄— CH₂CH₃ H(l = O) SC₆H₅ 1064 —(CH₂)₅— CH₂CH₃ H(l = O) SC₆H₅ 1065 H H CF₃ H(l = O) SC₆H₅ 1066 CH₃ CH₃ CF₃ H(l = O) SC₆H₅ 1067 CH₂CH₃ CH₂CH₃ CF₃ H(l = O) SC₆H₅ 1068 CH₂CH₂CH₃ CH₂CH₂CH₃ CF₃ H(l = O) SC₆H₅ 1069 OCH₃ OCH₃ CF₃ H(l = O) SC₆H₅ 1070 OCH₂CH₃ OCH₂CH₃ CF₃ H(l = O) SC₆H₅ 1071 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CF₃ H(l = O) SC₆H₅ 1072 SCH₃ SCH₃ CF₃ H(l = O) SC₆H₅ 1073 SCH₂CH₃ SCH₂CH₃ CF₃ H(l = O) SC₆H₅ 1074 N(CH₃)₂ N(CH₃)₂ CF₃ H(l = O) SC₆H₅ 1075 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CF₃ H(l = O) SC₆H₅ 1076 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CF₃ H(l = O) SC₆H₅ 1077 O—(CH₂CH₂)—O CF₃ H(l = O) SC₆H₅ 1078 O—(CH₂CH₂CH₂)—O CF₃ H(l = O) SC₆H₅ 1079 S—(CH₂CH₂)—S CF₃ H(l = O) SC₆H₅ 1080 S—(CH₂CH₂CH₂)—S CF₃ H(l = O) SC₆H₅ 1081 —(CH₂)₄— CF₃ H(l = O) SC₆H₅ 1082 —(CH₂)₅— CF₃ H(l = O) SC₆H₅ 1083 H H OCH₃ H(l = O) SC₆H₅ 1084 CH₃ CH₃ OCH₃ H(l = O) SC₆H₅ 1085 CH₂CH₃ CH₂CH₃ OCH₃ H(l = O) SC₆H₅ 1086 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₃ H(l = O) SC₆H₅ 1087 OCH₃ OCH₃ OCH₃ H(l = O) SC₆H₅ 1088 OCH₂CH₃ OCH₂CH₃ OCH₃ H(l = O) SC₆H₅ 1089 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₃ H(l = O) SC₆H₅ 1090 SCH₃ SCH₃ OCH₃ H(l = O) SC₆H₅ 1091 SCH₂CH₃ SCH₂CH₃ OCH₃ H(l = O) SC₆H₅ 1092 N(CH₃)₂ N(CH₃)₂ OCH₃ H(l = O) SC₆H₅ 1093 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₃ H(l = O) SC₆H₅ 1094 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₃ H(l = O) SC₆H₅ 1095 O—(CH₂CH₂)—O OCH₃ H(l = O) SC₆H₅ 1096 O—(CH₂CH₂CH₂)—O OCH₃ H(l = O) SC₆H₅ 1097 S—(CH₂CH₂)—S OCH₃ H(l = O) SC₆H₅ 1098 S—(CH₂CH₂CH₂)—S OCH₃ H(l = O) SC₆H₅ 1099 —(CH₂)₄— OCH₃ H(l = O) SC₆H₅ 1100 —(CH₂)₅— OCH₃ H(l = O) SC₆H₅ 1101 H H OCH₂CH₃ H(l = O) SC₆H₅ 1102 CH₃ CH₃ OCH₂CH₃ H(l = O) SC₆H₅ 1103 CH₂CH₃ CH₂CH₃ OCH₂CH₃ H(l = O) SC₆H₅ 1104 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₂CH₃ H(l = O) SC₆H₅ 1105 OCH₃ OCH₃ OCH₂CH₃ H(l = O) SC₆H₅ 1106 OCH₂CH₃ OCH₂CH₃ OCH₂CH₃ H(l = O) SC₆H₅ 1107 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₂CH₃ H(l = O) SC₆H₅ 1108 SCH₃ SCH₃ OCH₂CH₃ H(l = O) SC₆H₅ 1109 SCH₂CH₃ SCH₂CH₃ OCH₂CH₃ H(l = O) SC₆H₅ 1110 N(CH₃)₂ N(CH₃)₂ OCH₂CH₃ H(l = O) SC₆H₅ 1111 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₂CH₃ H(l = O) SC₆H₅ 1112 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₂CH₃ H(l = O) SC₆H₅ 1113 O—(CH₂CH₂)—O OCH₂CH₃ H(l = O) SC₆H₅ 1114 O—(CH₂CH₂CH₂)—O OCH₂CH₃ H(l = O) SC₆H₅ 1115 S—(CH₂CH₂)—S OCH₂CH₃ H(l = O) SC₆H₅ 1116 S—(CH₂CH₂CH₂)—S OCH₂CH₃ H(l = O) SC₆H₅ 1117 —(CH₂)₄— OCH₂CH₃ H(l = O) SC₆H₅ 1118 —(CH₂)₅— OCH₂CH₃ H(l = O) SC₆H₅ 1119 H H SCH₃ H(l = O) SC₆H₅ 1120 CH₃ CH₃ SCH₃ H(l = O) SC₆H₅ 1121 CH₂CH₃ CH₂CH₃ SCH₃ H(l = O) SC₆H₅ 1122 CH₂CH₂CH₃ CH₂CH₂CH₃ SCH₃ H(l = O) SC₆H₅ 1123 OCH₃ OCH₃ SCH₃ H(l = O) SC₆H₅ 1124 OCH₂CH₃ OCH₂CH₃ SCH₃ H(l = O) SC₆H₅ 1125 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SCH₃ H(l = O) SC₆H₅ 1126 SCH₃ SCH₃ SCH₃ H(l = O) SC₆H₅ 1127 SCH₂CH₃ SCH₂CH₃ SCH₃ H(l = O) SC₆H₅ 1128 N(CH₃)₂ N(CH₃)₂ SCH₃ H(l = O) SC₆H₅ 1129 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SCH₃ H(l = O) SC₆H₅ 1130 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SCH₃ H(l = O) SC₆H₅ 1131 O—(CH₂CH₂)—O SCH₃ H(l = O) SC₆H₅ 1132 O—(CH₂CH₂CH₂)—O SCH₃ H(l = O) SC₆H₅ 1133 S—(CH₂CH₂)—S SCH₃ H(l = O) SC₆H₅ 1134 S—(CH₂CH₂CH₂)—S SCH₃ H(l = O) SC₆H₅ 1135 —(CH₂)₄— SCH₃ H(l = O) SC₆H₅ 1136 —(CH₂)₅— SCH₃ H(l = O) SC₆H₅ 1137 H H SO₂CH₃ H(l = O) SC₆H₅ 1138 CH₃ CH₃ SO₂CH₃ H(l = O) SC₆H₅ 1139 CH₂CH₃ CH₂CH₃ SO₂CH₃ H(l = O) SC₆H₅ 1140 CH₂CH₂CH₃ CH₂CH₂CH₃ SO₂CH₃ H(l = O) SC₆H₅ 1141 OCH₃ OCH₃ SO₂CH₃ H(l = O) SC₆H₅ 1142 OCH₂CH₃ OCH₂CH₃ SO₂CH₃ H(l = O) SC₆H₅ 1143 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SO₂CH₃ H(l = O) SC₆H₅ 1144 SCH₃ SCH₃ SO₂CH₃ H(l = O) SC₆H₅ 1145 SCH₂CH₃ SCH₂CH₃ SO₂CH₃ H(l = O) SC₆H₅ 1146 N(CH₃)₂ N(CH₃)₂ SO₂CH₃ H(l = O) SC₆H₅ 1147 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SO₂CH₃ H(l = O) SC₆H₅ 1148 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SO₂CH₃ H(l = O) SC₆H₅ 1149 O—(CH₂CH₂)—O SO₂CH₃ H(l = O) SC₆H₅ 1150 O—(CH₂CH₂CH₂)—O SO₂CH₃ H(l = O) SC₆H₅ 1151 S—(CH₂CH₂)—S SO₂CH₃ H(l = O) SC₆H₅ 1152 S—(CH₂CH₂CH₂)—S SO₂CH₃ H(l = O) SC₆H₅ 1153 —(CH₂)₄— SO₂CH₃ H(l = O) SC₆H₅ 1154 —(CH₂)₅— SO₂CH₃ H(l = O) SC₆H₅ 1155 H H PO(OCH₃)₂ H(l = O) SC₆H₅ 1156 CH₃ CH₃ PO(OCH₃)₂ H(l = O) SC₆H₅ 1157 CH₂CH₃ CH₂CH₃ PO(OCH₃)₂ H(l = O) SC₆H₅ 1158 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₃)₂ H(l = O) SC₆H₅ 1159 OCH₃ OCH₃ PO(OCH₃)₂ H(l = O) SC₆H₅ 1160 OCH₂CH₃ OCH₂CH₃ PO(OCH₃)₂ H(l = O) SC₆H₅ 1161 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₃)₂ H(l = O) SC₆H₅ 1162 SCH₃ SCH₃ PO(OCH₃)₂ H(l = O) SC₆H₅ 1163 SCH₂CH₃ SCH₂CH₃ PO(OCH₃)₂ H(l = O) SC₆H₅ 1164 N(CH₃)₂ N(CH₃)₂ PO(OCH₃)₂ H(l = O) SC₆H₅ 1165 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₃)₂ H(l = O) SC₆H₅ 1166 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₃)₂ H(l = O) SC₆H₅ 1167 O—(CH₂CH₂)—O PO(OCH₃)₂ H(l = O) SC₆H₅ 1168 O—(CH₂CH₂CH₂)—O PO(OCH₃)₂ H(l = O) SC₆H₅ 1169 S—(CH₂CH₂)—S PO(OCH₃)₂ H(l = O) SC₆H₅ 1170 S—(CH₂CH₂CH₂)—S PO(OCH₃)₂ H(l = O) SC₆H₅ 1171 —(CH₂)₄— PO(OCH₃)₂ H(l = O) SC₆H₅ 1172 —(CH₂)₅— PO(OCH₃)₂ H(l = O) SC₆H₅ 1173 H H PO(OCH₂CH₃)₂ H(l = O) SC₆H₅ 1174 CH₃ CH₃ PO(OCH₂CH₃)₂ H(l = O) SC₆H₅ 1175 CH₂CH₃ CH₂CH₃ PO(OCH₂CH₃)₂ H(l = O) SC₆H₅ 1176 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₂CH₃)₂ H(l = O) SC₆H₅ 1177 OCH₃ OCH₃ PO(OCH₂CH₃)₂ H(l = O) SC₆H₅ 1178 OCH₂CH₃ OCH₂CH₃ PO(OCH₂CH₃)₂ H(l = O) SC₆H₅ 1179 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₂CH₃)₂ H(l = O) SC₆H₅ 1180 SCH₃ SCH₃ PO(OCH₂CH₃)₂ H(l = O) SC₆H₅ 1181 SCH₂CH₃ SCH₂CH₃ PO(OCH₂CH₃)₂ H(l = O) SC₆H₅ 1182 N(CH₃)₂ N(CH₃)₂ PO(OCH₂CH₃)₂ H(l = O) SC₆H₅ 1183 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₂CH₃)₂ H(l = O) SC₆H₅ 1184 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₂CH₃)₂ H(l = O) SC₆H₅ 1185 O—(CH₂CH₂)—O PO(OCH₂CH₃)₂ H(l = O) SC₆H₅ 1186 O—(CH₂CH₂CH₂)—O PO(OCH₂CH₃)₂ H(l = O) SC₆H₅ 1187 S—(CH₂CH₂)—S PO(OCH₂CH₃)₂ H(l = O) SC₆H₅ 1188 S—(CH₂CH₂CH₂)—S PO(OCH₂CH₃)₂ H(l = O) SC₆H₅ 1189 —(CH₂)₄— PO(OCH₂CH₃)₂ H(l = O) SC₆H₅ 1190 —(CH₂)₅— PO(OCH₂CH₃)₂ H(l = O) SC₆H₅ 1191 H H PO(CH₃)₂ H(l = O) SC₆H₅ 1192 CH₃ CH₃ PO(CH₃)₂ H(l = O) SC₆H₅ 1193 CH₂CH₃ CH₂CH₃ PO(CH₃)₂ H(l = O) SC₆H₅ 1194 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₃)₂ H(l = O) SC₆H₅ 1195 OCH₃ OCH₃ PO(CH₃)₂ H(l = O) SC₆H₅ 1196 OCH₂CH₃ OCH₂CH₃ PO(CH₃)₂ H(l = O) SC₆H₅ 1197 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₃)₂ H(l = O) SC₆H₅ 1198 SCH₃ SCH₃ PO(CH₃)₂ H(l = O) SC₆H₅ 1199 SCH₂CH₃ SCH₂CH₃ PO(CH₃)₂ H(l = O) SC₆H₅ 1200 N(CH₃)₂ N(CH₃)₂ PO(CH₃)₂ H(l = O) SC₆H₅ 1201 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₃)₂ H(l = O) SC₆H₅ 1202 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₃)₂ H(l = O) SC₆H₅ 1203 O—(CH₂CH₂)—O PO(CH₃)₂ H(l = O) SC₆H₅ 1204 O—(CH₂CH₂CH₂)—O PO(CH₃)₂ H(l = O) SC₆H₅ 1205 S—(CH₂CH₂)—S PO(CH₃)₂ H(l = O) SC₆H₅ 1206 S—(CH₂CH₂CH₂)—S PO(CH₃)₂ H(l = O) SC₆H₅ 1207 —(CH₂)₄— PO(CH₃)₂ H(l = O) SC₆H₅ 1208 —(CH₂)₅— PO(CH₃)₂ H(l = O) SC₆H₅ 1209 H H PO(CH₂CH₃)₂ H(l = O) SC₆H₅ 1210 CH₃ CH₃ PO(CH₂CH₃)₂ H(l = O) SC₆H₅ 1211 CH₂CH₃ CH₂CH₃ PO(CH₂CH₃)₂ H(l = O) SC₆H₅ 1212 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₂CH₃)₂ H(l = O) SC₆H₅ 1213 OCH₃ OCH₃ PO(CH₂CH₃)₂ H(l = O) SC₆H₅ 1214 OCH₂CH₃ OCH₂CH₃ PO(CH₂CH₃)₂ H(l = O) SC₆H₅ 1215 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₂CH₃)₂ H(l = O) SC₆H₅ 1216 SCH₃ SCH₃ PO(CH₂CH₃)₂ H(l = O) SC₆H₅ 1217 SCH₂CH₃ SCH₂CH₃ PO(CH₂CH₃)₂ H(l = O) SC₆H₅ 1218 N(CH₃)₂ N(CH₃)₂ PO(CH₂CH₃)₂ H(l = O) SC₆H₅ 1219 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₂CH₃)₂ H(l = O) SC₆H₅ 1220 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₂CH₃)₂ H(l = O) SC₆H₅ 1221 O—(CH₂CH₂)—O PO(CH₂CH₃)₂ H(l = O) SC₆H₅ 1222 O—(CH₂CH₂CH₂)—O PO(CH₂CH₃)₂ H(l = O) SC₆H₅ 1223 S—(CH₂CH₂)—S PO(CH₂CH₃)₂ H(l = O) SC₆H₅ 1224 S—(CH₂CH₂CH₂)—S PO(CH₂CH₃)₂ H(l = O) SC₆H₅ 1225 —(CH₂)₄— PO(CH₂CH₃)₂ H(l = O) SC₆H₅ 1226 —(CH₂)₅— PO(CH₂CH₃)₂ H(l = O) SC₆H₅ 1227 H H H H(l = O) Het1 1228 CH₃ CH₃ H H(l = O) Het1 1229 CH₂CH₃ CH₂CH₃ H H(l = O) Het1 1230 CH₂CH₂CH₃ CH₂CH₂CH₃ H H(l = O) Het1 1231 OCH₃ OCH₃ H H(l = O) Het1 1232 OCH₂CH₃ OCH₂CH₃ H H(l = O) Het1 1233 OCH₂CH₂CH₃ OCH₂CH₂CH₃ H H(l = O) Het1 1234 SCH₃ SCH₃ H H(l = O) Het1 1235 SCH₂CH₃ SCH₂CH₃ H H(l = O) Het1 1236 N(CH₃)₂ N(CH₃)₂ H H(l = O) Het1 1237 N(CH₂CH₃)₂ N(CH₂CH₃)₂ H H(l = O) Het1 1238 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) H H(l = O) Het1 1239 O—(CH₂CH₂)—O H H(l = O) Het1 1240 O—(CH₂CH₂CH₂)—O H H(l = O) Het1 1241 S—(CH₂CH₂)—S H H(l = O) Het1 1242 S—(CH₂CH₂CH₂)—S H H(l = O) Het1 1243 —(CH₂)₄— H H(l = O) Het1 1244 —(CH₂)₅— H H(l = O) Het1 1245 H H NO₂ H(l = O) Het1 1246 CH₃ CH₃ NO₂ H(l = O) Het1 1247 CH₂CH₃ CH₂CH₃ NO₂ H(l = O) Het1 1248 CH₂CH₂CH₃ CH₂CH₂CH₃ NO₂ H(l = O) Het1 1249 OCH₃ OCH₃ NO₂ H(l = O) Het1 1250 OCH₂CH₃ OCH₂CH₃ NO₂ H(l = O) Het1 1251 OCH₂CH₂CH₃ OCH₂CH₂CH₃ NO₂ H(l = O) Het1 1252 SCH₃ SCH₃ NO₂ H(l = O) Het1 1253 SCH₂CH₃ SCH₂CH₃ NO₂ H(l = O) Het1 1254 N(CH₃)₂ N(CH₃)₂ NO₂ H(l = O) Het1 1255 N(CH₂CH₃)₂ N(CH₂CH₃)₂ NO₂ H(l = O) Het1 1256 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) NO₂ H(l = O) Het1 1257 O—(CH₂CH₂)—O NO₂ H(l = O) Het1 1258 O—(CH₂CH₂CH₂)—O NO₂ H(l = O) Het1 1259 S—(CH₂CH₂)—S NO₂ H(l = O) Het1 1260 S—(CH₂CH₂CH₂)—S NO₂ H(l = O) Het1 1261 —(CH₂)₄— NO₂ H(l = O) Het1 1262 —(CH₂)₅— NO₂ H(l = O) Het1 1263 H H CN H(l = O) Het1 1264 CH₃ CH₃ CN H(l = O) Het1 1265 CH₂CH₃ CH₂CH₃ CN H(l = O) Het1 1266 CH₂CH₂CH₃ CH₂CH₂CH₃ CN H(l = O) Het1 1267 OCH₃ OCH₃ CN H(l = O) Het1 1268 OCH₂CH₃ OCH₂CH₃ CN H(l = O) Het1 1269 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CN H(l = O) Het1 1270 SCH₃ SCH₃ CN H(l = O) Het1 1271 SCH₂CH₃ SCH₂CH₃ CN H(l = O) Het1 1272 N(CH₃)₂ N(CH₃)₂ CN H(l = O) Het1 1273 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CN H(l = O) Het1 1274 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CN H(l = O) Het1 1275 O—(CH₂CH₂)—O CN H(l = O) Het1 1276 O—(CH₂CH₂CH₂)—O CN H(l = O) Het1 1277 S—(CH₂CH₂)—S CN H(l = O) Het1 1278 S—(CH₂CH₂CH₂)—S CN H(l = O) Het1 1279 —(CH₂)₄— CN H(l = O) Het1 1280 —(CH₂)₅— CN H(l = O) Het1 1281 H H F H(l = O) Het1 1282 CH₃ CH₃ F H(l = O) Het1 1283 CH₂CH₃ CH₂CH₃ F H(l = O) Het1 1284 CH₂CH₂CH₃ CH₂CH₂CH₃ F H(l = O) Het1 1285 OCH₃ OCH₃ F H(l = O) Het1 1286 OCH₂CH₃ OCH₂CH₃ F H(l = O) Het1 1287 OCH₂CH₂CH₃ OCH₂CH₂CH₃ F H(l = O) Het1 1288 SCH₃ SCH₃ F H(l = O) Het1 1289 SCH₂CH₃ SCH₂CH₃ F H(l = O) Het1 1290 N(CH₃)₂ N(CH₃)₂ F H(l = O) Het1 1291 N(CH₂CH₃)₂ N(CH₂CH₃)₂ F H(l = O) Het1 1292 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) F H(l = O) Het1 1293 O—(CH₂CH₂)—O F H(l = O) Het1 1294 O—(CH₂CH₂CH₂)—O F H(l = O) Het1 1295 S—(CH₂CH₂)—S F H(l = O) Het1 1296 S—(CH₂CH₂CH₂)—S F H(l = O) Het1 1297 —(CH₂)₄— F H(l = O) Het1 1298 —(CH₂)₅— F H(l = O) Het1 1299 H H Cl H(l = O) Het1 1300 CH₃ CH₃ Cl H(l = O) Het1 1301 CH₂CH₃ CH₂CH₃ Cl H(l = O) Het1 1302 CH₂CH₂CH₃ CH₂CH₂CH₃ Cl H(l = O) Het1 1303 OCH₃ OCH₃ Cl H(l = O) Het1 1304 OCH₂CH₃ OCH₂CH₃ Cl H(l = O) Het1 1305 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Cl H(l = O) Het1 1306 SCH₃ SCH₃ Cl H(l = O) Het1 1307 SCH₂CH₃ SCH₂CH₃ Cl H(l = O) Het1 1308 N(CH₃)₂ N(CH₃)₂ Cl H(l = O) Het1 1309 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Cl H(l = O) Het1 1310 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Cl H(l = O) Het1 1311 O—(CH₂CH₂)—O Cl H(l = O) Het1 1312 O—(CH₂CH₂CH₂)—O Cl H(l = O) Het1 1313 S—(CH₂CH₂)—S Cl H(l = O) Het1 1314 S—(CH₂CH₂CH₂)—S H(l = O) Het1 1315 —(CH₂)₄— Cl H(l = O) Het1 1316 —(CH₂)₅— Cl H(l = O) Het1 1317 H H Br H(l = O) Het1 1318 CH₃ CH₃ Br H(l = O) Het1 1319 CH₂CH₃ CH₂CH₃ Br H(l = O) Het1 1320 CH₂CH₂CH₃ CH₂CH₂CH₃ Br H(l = O) Het1 1321 OCH₃ OCH₃ Br H(l = O) Het1 1322 OCH₂CH₃ OCH₂CH₃ Br H(l = O) Het1 1323 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Br H(l = O) Het1 1324 SCH₃ SCH₃ Br H(l = O) Het1 1325 SCH₂CH₃ SCH₂CH₃ Br H(l = O) Het1 1326 N(CH₃)₂ N(CH₃)₂ Br H(l = O) Het1 1327 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Br H(l = O) Het1 1328 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Br H(l = O) Het1 1329 O—(CH₂CH₂)—O Br H(l = O) Het1 1330 O—(CH₂CH₂CH₂)—O Br H(l = O) Het1 1331 S—(CH₂CH₂)—S Br H(l = O) Het1 1332 S—(CH₂CH₂CH₂)—S Br H(l = O) Het1 1333 —(CH₂)₄— Br H(l = O) Het1 1334 —(CH₂)₅— Br H(l = O) Het1 1335 H H CH₃ H(l = O) Het1 1336 CH₃ CH₃ CH₃ H(l = O) Het1 1337 CH₂CH₃ CH₂CH₃ CH₃ H(l = O) Het1 1338 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₃ H(l = O) Het1 1339 OCH₃ OCH₃ CH₃ H(l = O) Het1 1340 OCH₂CH₃ OCH₂CH₃ CH₃ H(l = O) Het1 1341 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₃ H(l = O) Het1 1342 SCH₃ SCH₃ CH₃ H(l = O) Het1 1343 SCH₂CH₃ SCH₂CH₃ CH₃ H(l = O) Het1 1344 N(CH₃)₂ N(CH₃)₂ CH₃ H(l = O) Het1 1345 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₃ H(l = O) Het1 1346 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₃ H(l = O) Het1 1347 O—(CH₂CH₂)—O CH₃ H(l = O) Het1 1348 O—(CH₂CH₂CH₂)—O CH₃ H(l = O) Het1 1349 S—(CH₂CH₂)—S CH₃ H(l = O) Het1 1350 S—(CH₂CH₂CH₂)—S CH₃ H(l = O) Het1 1351 —(CH₂)₄— CH₃ H(l = O) Het1 1352 —(CH₂)₅— CH₃ H(l = O) Het1 1353 H H CH₂CH₃ H(l = O) Het1 1354 CH₃ CH₃ CH₂CH₃ H(l = O) Het1 1355 CH₂CH₃ CH₂CH₃ CH₂CH₃ H(l = O) Het1 1356 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₂CH₃ H(l = O) Het1 1357 OCH₃ OCH₃ CH₂CH₃ H(l = O) Het1 1358 OCH₂CH₃ OCH₂CH₃ CH₂CH₃ H(l = O) Het1 1359 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₂CH₃ H(l = O) Het1 1360 SCH₃ SCH₃ CH₂CH₃ H(l = O) Het1 1361 SCH₂CH₃ SCH₂CH₃ CH₂CH₃ H(l = O) Het1 1362 N(CH₃)₂ N(CH₃)₂ CH₂CH₃ H(l = O) Het1 1363 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₂CH₃ H(l = O) Het1 1364 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₂CH₃ H(l = O) Het1 1365 O—(CH₂CH₂)—O CH₂CH₃ H(l = O) Het1 1366 O—(CH₂CH₂CH₂)—O CH₂CH₃ H(l = O) Het1 1367 S—(CH₂CH₂)—S CH₂CH₃ H(l = O) Het1 1368 S—(CH₂CH₂CH₂)—S CH₂CH₃ H(l = O) Het1 1369 —(CH₂)₄— CH₂CH₃ H(l = O) Het1 1370 —(CH₂)₅— CH₂CH₃ H(l = O) Het1 1371 H H CF₃ H(l = O) Het1 1372 CH₃ CH₃ CF₃ H(l = O) Het1 1373 CH₂CH₃ CH₂CH₃ CF₃ H(l = O) Het1 1374 CH₂CH₂CH₃ CH₂CH₂CH₃ CF₃ H(l = O) Het1 1375 OCH₃ OCH₃ CF₃ H(l = O) Het1 1376 OCH₂CH₃ OCH₂CH₃ CF₃ H(l = O) Het1 1377 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CF₃ H(l = O) Het1 1378 SCH₃ SCH₃ CF₃ H(l = O) Het1 1379 SCH₂CH₃ SCH₂CH₃ CF₃ H(l = O) Het1 1380 N(CH₃)₂ N(CH₃)₂ CF₃ H(l = O) Het1 1381 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CF₃ H(l = O) Het1 1382 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CF₃ H(l = O) Het1 1383 O—(CH₂CH₂)—O CF₃ H(l = O) Het1 1384 O—(CH₂CH₂CH₂)—O CF₃ H(l = O) Het1 1385 S—(CH₂CH₂)—S CF₃ H(l = O) Het1 1386 S—(CH₂CH₂CH₂)—S CF₃ H(l = O) Het1 1387 —(CH₂)₄— CF₃ H(l = O) Het1 1388 —(CH₂)₅— CF₃ H(l = O) Het1 1389 H H OCH₃ H(l = O) Het1 1390 CH₃ CH₃ OCH₃ H(l = O) Het1 1391 CH₂CH₃ CH₂CH₃ OCH₃ H(l = O) Het1 1392 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₃ H(l = O) Het1 1393 OCH₃ OCH₃ OCH₃ H(l = O) Het1 1394 OCH₂CH₃ OCH₂CH₃ OCH₃ H(l = O) Het1 1395 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₃ H(l = O) Het1 1396 SCH₃ SCH₃ OCH₃ H(l = O) Het1 1397 SCH₂CH₃ SCH₂CH₃ OCH₃ H(l = O) Het1 1398 N(CH₃)₂ N(CH₃)₂ OCH₃ H(l = O) Het1 1399 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₃ H(l = O) Het1 1400 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₃ H(l = O) Het1 1401 O—(CH₂CH₂)—O OCH₃ H(l = O) Het1 1402 O—(CH₂CH₂CH₂)—O OCH₃ H(l = O) Het1 1403 S—(CH₂CH₂)—S OCH₃ H(l = O) Het1 1404 S—(CH₂CH₂CH₂)—S OCH₃ H(l = O) Het1 1405 —(CH₂)₄— OCH₃ H(l = O) Het1 1406 —(CH₂)₅— OCH₃ H(l = O) Het1 1407 H H OCH₂CH₃ H(l = O) Het1 1408 CH₃ CH₃ OCH₂CH₃ H(l = O) Het1 1409 CH₂CH₃ CH₂CH₃ OCH₂CH₃ H(l = O) Het1 1410 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₂CH₃ H(l = O) Het1 1411 OCH₃ OCH₃ OCH₂CH₃ H(l = O) Het1 1412 OCH₂CH₃ OCH₂CH₃ OCH₂CH₃ H(l = O) Het1 1413 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₂CH₃ H(l = O) Het1 1414 SCH₃ SCH₃ OCH₂CH₃ H(l = O) Het1 1415 SCH₂CH₃ SCH₂CH₃ OCH₂CH₃ H(l = O) Het1 1416 N(CH₃)₂ N(CH₃)₂ OCH₂CH₃ H(l = O) Het1 1417 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₂CH₃ H(l = O) Het1 1418 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₂CH₃ H(l = O) Het1 1419 O—(CH₂CH₂)—O OCH₂CH₃ H(l = O) Het1 1420 O—(CH₂CH₂CH₂)—O OCH₂CH₃ H(l = O) Het1 1421 S—(CH₂CH₂)—S OCH₂CH₃ H(l = O) Het1 1422 S—(CH₂CH₂CH₂)—S OCH₂CH₃ H(l = O) Het1 1423 —(CH₂)₄— OCH₂CH₃ H(l = O) Het1 1424 —(CH₂)₅— OCH₂CH₃ H(l = O) Het1 1425 H H SCH₃ H(l = O) Het1 1426 CH₃ CH₃ SCH₃ H(l = O) Het1 1427 CH₂CH₃ CH₂CH₃ SCH₃ H(l = O) Het1 1428 CH₂CH₂CH₃ CH₂CH₂CH₃ SCH₃ H(l = O) Het1 1429 OCH₃ OCH₃ SCH₃ H(l = O) Het1 1430 OCH₂CH₃ OCH₂CH₃ SCH₃ H(l = O) Het1 1431 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SCH₃ H(l = O) Het1 1432 SCH₃ SCH₃ SCH₃ H(l = O) Het1 1433 SCH₂CH₃ SCH₂CH₃ SCH₃ H(l = O) Het1 1434 N(CH₃)₂ N(CH₃)₂ SCH₃ H(l = O) Het1 1435 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SCH₃ H(l = O) Het1 1436 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SCH₃ H(l = O) Het1 1437 O—(CH₂CH₂)—O SCH₃ H(l = O) Het1 1438 O—(CH₂CH₂CH₂)—O SCH₃ H(l = O) Het1 1439 S—(CH₂CH₂)—S SCH₃ H(l = O) Het1 1440 S—(CH₂CH₂CH₂)—S H(l = O) Het1 1441 —(CH₂)₄— SCH₃ H(l = O) Het1 1442 —(CH₂)₅— SCH₃ H(l = O) Het1 1443 H H SO₂CH₃ H(l = O) Het1 1444 CH₃ CH₃ SO₂CH₃ H(l = O) Het1 1445 CH₂CH₃ CH₂CH₃ SO₂CH₃ H(l = O) Het1 1446 CH₂CH₂CH₃ CH₂CH₂CH₃ SO₂CH₃ H(l = O) Het1 1447 OCH₃ OCH₃ SO₂CH₃ H(l = O) Het1 1448 OCH₂CH₃ OCH₂CH₃ SO₂CH₃ H(l = O) Het1 1449 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SO₂CH₃ H(l = O) Het1 1450 SCH₃ SCH₃ SO₂CH₃ H(l = O) Het1 1451 SCH₂CH₃ SCH₂CH₃ SO₂CH₃ H(l = O) Het1 1452 N(CH₃)₂ N(CH₃)₂ SO₂CH₃ H(l = O) Het1 1453 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SO₂CH₃ H(l = O) Het1 1454 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SO₂CH₃ H(l = O) Het1 1455 O—(CH₂CH₂)—O SO₂CH₃ H(l = O) Het1 1456 O—(CH₂CH₂CH₂)—O SO₂CH₃ H(l = O) Het1 1457 S—(CH₂CH₂)—S SO₂CH₃ H(l = O) Het1 1458 S—(CH₂CH₂CH₂)—S SO₂CH₃ H(l = O) Het1 1459 —(CH₂)₄— SO₂CH₃ H(l = O) Het1 1460 —(CH₂)₅— SO₂CH₃ H(l = O) Het1 1461 H H PO(OCH₃)₂ H(l = O) Het1 1462 CH₃ CH₃ PO(OCH₃)₂ H(l = O) Het1 1463 CH₂CH₃ CH₂CH₃ PO(OCH₃)₂ H(l = O) Het1 1464 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₃)₂ H(l = O) Het1 1465 OCH₃ OCH₃ PO(OCH₃)₂ H(l = O) Het1 1466 OCH₂CH₃ OCH₂CH₃ PO(OCH₃)₂ H(l = O) Het1 1467 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₃)₂ H(l = O) Het1 1468 SCH₃ SCH₃ PO(OCH₃)₂ H(l = O) Het1 1469 SCH₂CH₃ SCH₂CH₃ PO(OCH₃)₂ H(l = O) Het1 1470 N(CH₃)₂ N(CH₃)₂ PO(OCH₃)₂ H(l = O) Het1 1471 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₃)₂ H(l = O) Het1 1472 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₃)₂ H(l = O) Het1 1473 O—(CH₂CH₂)—O PO(OCH₃)₂ H(l = O) Het1 1474 O—(CH₂CH₂CH₂)—O PO(OCH₃)₂ H(l = O) Het1 1475 S—(CH₂CH₂)—S PO(OCH₃)₂ H(l = O) Het1 1476 S—(CH₂CH₂CH₂)—S PO(OCH₃)₂ H(l = O) Het1 1477 —(CH₂)₄— PO(OCH₃)₂ H(l = O) Het1 1478 —(CH₂)₅— PO(OCH₃)₂ H(l = O) Het1 1479 H H PO(OCH₂CH₃)₂ H(l = O) Het1 1480 CH₃ CH₃ PO(OCH₂CH₃)₂ H(l = O) Het1 1481 CH₂CH₃ CH₂CH₃ PO(OCH₂CH₃)₂ H(l = O) Het1 1482 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₂CH₃)₂ H(l = O) Het1 1483 OCH₃ OCH₃ PO(OCH₂CH₃)₂ H(l = O) Het1 1484 OCH₂CH₃ OCH₂CH₃ PO(OCH₂CH₃)₂ H(l = O) Het1 1485 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₂CH₃)₂ H(l = O) Het1 1486 SCH₃ SCH₃ PO(OCH₂CH₃)₂ H(l = O) Het1 1487 SCH₂CH₃ SCH₂CH₃ PO(OCH₂CH₃)₂ H(l = O) Het1 1488 N(CH₃)₂ N(CH₃)₂ PO(OCH₂CH₃)₂ H(l = O) Het1 1489 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₂CH₃)₂ H(l = O) Het1 1490 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₂CH₃)₂ H(l = O) Het1 1491 O—(CH₂CH₂)—O PO(OCH₂CH₃)₂ H(l = O) Het1 1492 O—(CH₂CH₂CH₂)—O PO(OCH₂CH₃)₂ H(l = O) Het1 1493 S—(CH₂CH₂)—S PO(OCH₂CH₃)₂ H(l = O) Het1 1494 S—(CH₂CH₂CH₂)—S PO(OCH₂CH₃)₂ H(l = O) Het1 1495 —(CH₂)₄— PO(OCH₂CH₃)₂ H(l = O) Het1 1496 —(CH₂)₅— PO(OCH₂CH₃)₂ H(l = O) Het1 1497 H H PO(CH₃)₂ H(l = O) Het1 1498 CH₃ CH₃ PO(CH₃)₂ H(l = O) Het1 1499 CH₂CH₃ CH₂CH₃ PO(CH₃)₂ H(l = O) Het1 1500 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₃)₂ H(l = O) Het1 1501 OCH₃ OCH₃ PO(CH₃)₂ H(l = O) Het1 1502 OCH₂CH₃ OCH₂CH₃ PO(CH₃)₂ H(l = O) Het1 1503 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₃)₂ H(l = O) Het1 1504 SCH₃ SCH₃ PO(CH₃)₂ H(l = O) Het1 1505 SCH₂CH₃ SCH₂CH₃ PO(CH₃)₂ H(l = O) Het1 1506 N(CH₃)₂ N(CH₃)₂ PO(CH₃)₂ H(l = O) Het1 1507 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₃)₂ H(l = O) Het1 1508 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₃)₂ H(l = O) Het1 1509 O—(CH₂CH₂)—O PO(CH₃)₂ H(l = O) Het1 1510 O—(CH₂CH₂CH₂)—O PO(CH₃)₂ H(l = O) Het1 1511 S—(CH₂CH₂)—S PO(CH₃)₂ H(l = O) Het1 1512 S—(CH₂CH₂CH₂)—S PO(CH₃)₂ H(l = O) Het1 1513 —(CH₂)₄— PO(CH₃)₂ H(l = O) Het1 1514 —(CH₂)₅— PO(CH₃)₂ H(l = O) Het1 1515 H H PO(CH₂CH₃)₂ H(l = O) Het1 1516 CH₃ CH₃ PO(CH₂CH₃)₂ H(l = O) Het1 1517 CH₂CH₃ CH₂CH₃ PO(CH₂CH₃)₂ H(l = O) Het1 1518 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₂CH₃)₂ H(l = O) Het1 1519 OCH₃ OCH₃ PO(CH₂CH₃)₂ H(l = O) Het1 1520 OCH₂CH₃ OCH₂CH₃ PO(CH₂CH₃)₂ H(l = O) Het1 1521 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₂CH₃)₂ H(l = O) Het1 1522 SCH₃ SCH₃ PO(CH₂CH₃)₂ H(l = O) Het1 1523 SCH₂CH₃ SCH₂CH₃ PO(CH₂CH₃)₂ H(l = O) Het1 1524 N(CH₃)₂ N(CH₃)₂ PO(CH₂CH₃)₂ H(l = O) Het1 1525 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₂CH₃)₂ H(l = O) Het1 1526 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₂CH₃)₂ H(l = O) Het1 1527 O—(CH₂CH₂)—O PO(CH₂CH₃)₂ H(l = O) Het1 1528 O—(CH₂CH₂CH₂)—O PO(CH₂CH₃)₂ H(l = O) Het1 1529 S—(CH₂CH₂)—S PO(CH₂CH₃)₂ H(l = O) Het1 1530 S—(CH₂CH₂CH₂)—S PO(CH₂CH₃)₂ H(l = O) Het1 1531 —(CH₂)₄— PO(CH₂CH₃)₂ H(l = O) Het1 1532 —(CH₂)₅— PO(CH₂CH₃)₂ H(l = O) Het1 1533 H H H H(l = O) Het2 1534 CH₃ CH₃ H H(l = O) Het2 1535 CH₂CH₃ CH₂CH₃ H H(l = O) Het2 1536 CH₂CH₂CH₃ CH₂CH₂CH₃ H H(l = O) Het2 1537 OCH₃ OCH₃ H H(l = O) Het2 1538 OCH₂CH₃ OCH₂CH₃ H H(l = O) Het2 1539 OCH₂CH₂CH₃ OCH₂CH₂CH₃ H H(l = O) Het2 1540 SCH₃ SCH₃ H H(l = O) Het2 1541 SCH₂CH₃ SCH₂CH₃ H H(l = O) Het2 1542 N(CH₃)₂ N(CH₃)₂ H H(l = O) Het2 1543 N(CH₂CH₃)₂ N(CH₂CH₃)₂ H H(l = O) Het2 1544 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) H H(l = O) Het2 1545 O—(CH₂CH₂)—O H H(l = O) Het2 1546 O—(CH₂CH₂CH₂)—O H H(l = O) Het2 1547 S—(CH₂CH₂)—S H H(l = O) Het2 1548 S—(CH₂CH₂CH₂)—S H H(l = O) Het2 1549 —(CH₂)₄— H H(l = O) Het2 1550 —(CH₂)₅— H H(l = O) Het2 1551 H H NO₂ H(l = O) Het2 1552 CH₃ CH₃ NO₂ H(l = O) Het2 1553 CH₂CH₃ CH₂CH₃ NO₂ H(l = O) Het2 1554 CH₂CH₂CH₃ CH₂CH₂CH₃ NO₂ H(l = O) Het2 1555 OCH₃ OCH₃ NO₂ H(l = O) Het2 1556 OCH₂CH₃ OCH₂CH₃ NO₂ H(l = O) Het2 1557 OCH₂CH₂CH₃ OCH₂CH₂CH₃ NO₂ H(l = O) Het2 1558 SCH₃ SCH₃ NO₂ H(l = O) Het2 1559 SCH₂CH₃ SCH₂CH₃ NO₂ H(l = O) Het2 1560 N(CH₃)₂ N(CH₃)₂ NO₂ H(l = O) Het2 1561 N(CH₂CH₃)₂ N(CH₂CH₃)₂ NO₂ H(l = O) Het2 1562 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) NO₂ H(l = O) Het2 1563 O—(CH₂CH₂)—O NO₂ H(l = O) Het2 1564 O—(CH₂CH₂CH₂)—O NO₂ H(l = O) Het2 1565 S—(CH₂CH₂)—S NO₂ H(l = O) Het2 1566 S—(CH₂CH₂CH₂)—S NO₂ H(l = O) Het2 1567 —(CH₂)₄— NO₂ H(l = O) Het2 1568 —(CH₂)₅— NO₂ H(l = O) Het2 1569 H H CN H(l = O) Het2 1570 CH₃ CH₃ CN H(l = O) Het2 1571 CH₂CH₃ CH₂CH₃ CN H(l = O) Het2 1572 CH₂CH₂CH₃ CH₂CH₂CH₃ CN H(l = O) Het2 1573 OCH₃ OCH₃ CN H(l = O) Het2 1574 OCH₂CH₃ OCH₂CH₃ CN H(l = O) Het2 1575 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CN H(l = O) Het2 1576 SCH₃ SCH₃ CN H(l = O) Het2 1577 SCH₂CH₃ SCH₂CH₃ CN H(l = O) Het2 1578 N(CH₃)₂ N(CH₃)₂ CN H(l = O) Het2 1579 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CN H(l = O) Het2 1580 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CN H(l = O) Het2 1581 O—(CH₂CH₂)—O CN H(l = O) Het2 1582 O—(CH₂CH₂CH₂)—O CN H(l = O) Het2 1583 S—(CH₂CH₂)—S CN H(l = O) Het2 1584 S—(CH₂CH₂CH₂)—S CN H(l = O) Het2 1585 —(CH₂)₄— CN H(l = O) Het2 1586 —(CH₂)₅— CN H(l = O) Het2 1587 H H F H(l = O) Het2 1588 CH₃ CH₃ F H(l = O) Het2 1589 CH₂CH₃ CH₂CH₃ F H(l = O) Het2 1590 CH₂CH₂CH₃ CH₂CH₂CH₃ F H(l = O) Het2 1591 OCH₃ OCH₃ F H(l = O) Het2 1592 OCH₂CH₃ OCH₂CH₃ F H(l = O) Het2 1593 OCH₂CH₂CH₃ OCH₂CH₂CH₃ F H(l = O) Het2 1594 SCH₃ SCH₃ F H(l = O) Het2 1595 SCH₂CH₃ SCH₂CH₃ F H(l = O) Het2 1596 N(CH₃)₂ N(CH₃)₂ F H(l = O) Het2 1597 N(CH₂CH₃)₂ N(CH₂CH₃)₂ F H(l = O) Het2 1598 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) F H(l = O) Het2 1599 O—(CH₂CH₂)—O F H(l = O) Het2 1600 O—(CH₂CH₂CH₂)—O F H(l = O) Het2 1601 S—(CH₂CH₂)—S F H(l = O) Het2 1602 S—(CH₂CH₂CH₂)—S F H(l = O) Het2 1603 —(CH₂)₄— F H(l = O) Het2 1604 —(CH₂)₅— F H(l = O) Het2 1605 H H Cl H(l = O) Het2 1606 CH₃ CH₃ Cl H(l = O) Het2 1607 CH₂CH₃ CH₂CH₃ Cl H(l = O) Het2 1608 CH₂CH₂CH₃ CH₂CH₂CH₃ Cl H(l = O) Het2 1609 OCH₃ OCH₃ Cl H(l = O) Het2 1610 OCH₂CH₃ OCH₂CH₃ Cl H(l = O) Het2 1611 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Cl H(l = O) Het2 1612 SCH₃ SCH₃ Cl H(l = O) Het2 1613 SCH₂CH₃ SCH₂CH₃ Cl H(l = O) Het2 1614 N(CH₃)₂ N(CH₃)₂ Cl H(l = O) Het2 1615 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Cl H(l = O) Het2 1616 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Cl H(l = O) Het2 1617 O—(CH₂CH₂)—O Cl H(l = O) Het2 1618 O—(CH₂CH₂CH₂)—O Cl H(l = O) Het2 1619 S—(CH₂CH₂)—S Cl H(l = O) Het2 1620 S—(CH₂CH₂CH₂)—S Cl H(l = O) Het2 1621 —(CH₂)₄— Cl H(l = O) Het2 1622 —(CH₂)₅— Cl H(l = O) Het2 1623 H H Br H(l = O) Het2 1624 CH₃ CH₃ Br H(l = O) Het2 1625 CH₂CH₃ CH₂CH₃ Br H(l = O) Het2 1626 CH₂CH₂CH₃ CH₂CH₂CH₃ Br H(l = O) Het2 1627 OCH₃ OCH₃ Br H(l = O) Het2 1628 OCH₂CH₃ OCH₂CH₃ Br H(l = O) Het2 1629 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Br H(l = O) Het2 1630 SCH₃ SCH₃ Br H(l = O) Het2 1631 SCH₂CH₃ SCH₂CH₃ Br H(l = O) Het2 1632 N(CH₃)₂ N(CH₃)₂ Br H(l = O) Het2 1633 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Br H(l = O) Het2 1634 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Br H(l = O) Het2 1635 O—(CH₂CH₂)—O Br H(l = O) Het2 1636 O—(CH₂CH₂CH₂)—O Br H(l = O) Het2 1637 S—(CH₂CH₂)—S Br H(l = O) Het2 1638 S—(CH₂CH₂CH₂)—S Br H(l = O) Het2 1639 —(CH₂)₄— Br H(l = O) Het2 1640 —(CH₂)₅— Br H(l = O) Het2 1641 H H CH₃ H(l = O) Het2 1642 CH₃ CH₃ CH₃ H(l = O) Het2 1643 CH₂CH₃ CH₂CH₃ CH₃ H(l = O) Het2 1644 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₃ H(l = O) Het2 1645 OCH₃ OCH₃ CH₃ H(l = O) Het2 1646 OCH₂CH₃ OCH₂CH₃ CH₃ H(l = O) Het2 1647 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₃ H(l = O) Het2 1648 SCH₃ SCH₃ CH₃ H(l = O) Het2 1649 SCH₂CH₃ SCH₂CH₃ CH₃ H(l = O) Het2 1650 N(CH₃)₂ N(CH₃)₂ CH₃ H(l = O) Het2 1651 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₃ H(l = O) Het2 1652 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₃ H(l = O) Het2 1653 O—(CH₂CH₂)—O CH₃ H(l = O) Het2 1654 O—(CH₂CH₂CH₂)—O CH₃ H(l = O) Het2 1655 S—(CH₂CH₂)—S CH₃ H(l = O) Het2 1656 S—(CH₂CH₂CH₂)—S CH₃ H(l = O) Het2 1657 —(CH₂)₄— CH₃ H(l = O) Het2 1658 —(CH₂)₅— CH₃ H(l = O) Het2 1659 H H CH₂CH₃ H(l = O) Het2 1660 CH₃ CH₃ CH₂CH₃ H(l = O) Het2 1661 CH₂CH₃ CH₂CH₃ CH₂CH₃ H(l = O) Het2 1662 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₂CH₃ H(l = O) Het2 1663 OCH₃ OCH₃ CH₂CH₃ H(l = O) Het2 1664 OCH₂CH₃ OCH₂CH₃ CH₂CH₃ H(l = O) Het2 1665 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₂CH₃ H(l = O) Het2 1666 SCH₃ SCH₃ CH₂CH₃ H(l = O) Het2 1667 SCH₂CH₃ SCH₂CH₃ CH₂CH₃ H(l = O) Het2 1668 N(CH₃)₂ N(CH₃)₂ CH₂CH₃ H(l = O) Het2 1669 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₂CH₃ H(l = O) Het2 1670 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₂CH₃ H(l = O) Het2 1671 O—(CH₂CH₂)—O CH₂CH₃ H(l = O) Het2 1672 O—(CH₂CH₂CH₂)—O CH₂CH₃ H(l = O) Het2 1673 S—(CH₂CH₂)—S CH₂CH₃ H(l = O) Het2 1674 S—(CH₂CH₂CH₂)—S CH₂CH₃ H(l = O) Het2 1675 —(CH₂)₄— CH₂CH₃ H(l = O) Het2 1676 —(CH₂)₅— CH₂CH₃ H(l = O) Het2 1677 H H CF₃ H(l = O) Het2 1678 CH₃ CH₃ CF₃ H(l = O) Het2 1679 CH₂CH₃ CH₂CH₃ CF₃ H(l = O) Het2 1680 CH₂CH₂CH₃ CH₂CH₂CH₃ CF₃ H(l = O) Het2 1681 OCH₃ OCH₃ CF₃ H(l = O) Het2 1682 OCH₂CH₃ OCH₂CH₃ CF₃ H(l = O) Het2 1683 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CF₃ H(l = O) Het2 1684 SCH₃ SCH₃ CF₃ H(l = O) Het2 1685 SCH₂CH₃ SCH₂CH₃ CF₃ H(l = O) Het2 1686 N(CH₃)₂ N(CH₃)₂ CF₃ H(l = O) Het2 1687 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CF₃ H(l = O) Het2 1688 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CF₃ H(l = O) Het2 1689 O—(CH₂CH₂)—O CF₃ H(l = O) Het2 1690 O—(CH₂CH₂CH₂)—O CF₃ H(l = O) Het2 1691 S—(CH₂CH₂)—S CF₃ H(l = O) Het2 1692 S—(CH₂CH₂CH₂)—S CF₃ H(l = O) Het2 1693 —(CH₂)₄— CF₃ H(l = O) Het2 1694 —(CH₂)₅— CF₃ H(l = O) Het2 1695 H H OCH₃ H(l = O) Het2 1696 CH₃ CH₃ OCH₃ H(l = O) Het2 1697 CH₂CH₃ CH₂CH₃ OCH₃ H(l = O) Het2 1698 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₃ H(l = O) Het2 1699 OCH₃ OCH₃ OCH₃ H(l = O) Het2 1700 OCH₂CH₃ OCH₂CH₃ OCH₃ H(l = O) Het2 1701 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₃ H(l = O) Het2 1702 SCH₃ SCH₃ OCH₃ H(l = O) Het2 1703 SCH₂CH₃ SCH₂CH₃ OCH₃ H(l = O) Het2 1704 N(CH₃)₂ N(CH₃)₂ OCH₃ H(l = O) Het2 1705 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₃ H(l = O) Het2 1706 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₃ H(l = O) Het2 1707 O—(CH₂CH₂)—O OCH₃ H(l = O) Het2 1708 O—(CH₂CH₂CH₂)—O OCH₃ H(l = O) Het2 1709 S—(CH₂CH₂)—S OCH₃ H(l = O) Het2 1710 S—(CH₂CH₂CH₂)—S OCH₃ H(l = O) Het2 1711 —(CH₂)₄— OCH₃ H(l = O) Het2 1712 —(CH₂)₅— OCH₃ H(l = O) Het2 1713 H H OCH₂CH₃ H(l = O) Het2 1714 CH₃ CH₃ OCH₂CH₃ H(l = O) Het2 1715 CH₂CH₃ CH₂CH₃ OCH₂CH₃ H(l = O) Het2 1716 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₂CH₃ H(l = O) Het2 1717 OCH₃ OCH₃ OCH₂CH₃ H(l = O) Het2 1718 OCH₂CH₃ OCH₂CH₃ OCH₂CH₃ H(l = O) Het2 1719 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₂CH₃ H(l = O) Het2 1720 SCH₃ SCH₃ OCH₂CH₃ H(l = O) Het2 1721 SCH₂CH₃ SCH₂CH₃ OCH₂CH₃ H(l = O) Het2 1722 N(CH₃)₂ N(CH₃)₂ OCH₂CH₃ H(l = O) Het2 1723 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₂CH₃ H(l = O) Het2 1724 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₂CH₃ H(l = O) Het2 1725 O—(CH₂CH₂)—O OCH₂CH₃ H(l = O) Het2 1726 O—(CH₂CH₂CH₂)—O OCH₂CH₃ H(l = O) Het2 1727 S—(CH₂CH₂)—S OCH₂CH₃ H(l = O) Het2 1728 S—(CH₂CH₂CH₂)—S OCH₂CH₃ H(l = O) Het2 1729 —(CH₂)₄— OCH₂CH₃ H(l = O) Het2 1730 —(CH₂)₅— OCH₂CH₃ H(l = O) Het2 1731 H H SCH₃ H(l = O) Het2 1732 CH₃ CH₃ SCH₃ H(l = O) Het2 1733 CH₂CH₃ CH₂CH₃ SCH₃ H(l = O) Het2 1734 CH₂CH₂CH₃ CH₂CH₂CH₃ SCH₃ H(l = O) Het2 1735 OCH₃ OCH₃ SCH₃ H(l = O) Het2 1736 OCH₂CH₃ OCH₂CH₃ SCH₃ H(l = O) Het2 1737 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SCH₃ H(l = O) Het2 1738 SCH₃ SCH₃ SCH₃ H(l = O) Het2 1739 SCH₂CH₃ SCH₂CH₃ SCH₃ H(l = O) Het2 1740 N(CH₃)₂ N(CH₃)₂ SCH₃ H(l = O) Het2 1741 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SCH₃ H(l = O) Het2 1742 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SCH₃ H(l = O) Het2 1743 O—(CH₂CH₂)—O SCH₃ H(l = O) Het2 1744 O—(CH₂CH₂CH₂)—O SCH₃ H(l = O) Het2 1745 S—(CH₂CH₂)—S SCH₃ H(l = O) Het2 1746 S—(CH₂CH₂CH₂)—S SCH₃ H(l = O) Het2 1747 —(CH₂)₄— SCH₃ H(l = O) Het2 1748 —(CH₂)₅— SCH₃ H(l = O) Het2 1749 H H SO₂CH₃ H(l = O) Het2 1750 CH₃ CH₃ SO₂CH₃ H(l = O) Het2 1751 CH₂CH₃ CH₂CH₃ SO₂CH₃ H(l = O) Het2 1752 CH₂CH₂CH₃ CH₂CH₂CH₃ SO₂CH₃ H(l = O) Het2 1753 OCH₃ OCH₃ SO₂CH₃ H(l = O) Het2 1754 OCH₂CH₃ OCH₂CH₃ SO₂CH₃ H(l = O) Het2 1755 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SO₂CH₃ H(l = O) Het2 1756 SCH₃ SCH₃ SO₂CH₃ H(l = O) Het2 1757 SCH₂CH₃ SCH₂CH₃ SO₂CH₃ H(l = O) Het2 1758 N(CH₃)₂ N(CH₃)₂ SO₂CH₃ H(l = O) Het2 1759 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SO₂CH₃ H(l = O) Het2 1760 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SO₂CH₃ H(l = O) Het2 1761 O—(CH₂CH₂)—O SO₂CH₃ H(l = O) Het2 1762 O—(CH₂CH₂CH₂)—O SO₂CH₃ H(l = O) Het2 1763 S—(CH₂CH₂)—S SO₂CH₃ H(l = O) Het2 1764 S—(CH₂CH₂CH₂)—S SO₂CH₃ H(l = O) Het2 1765 —(CH₂)₄— SO₂CH₃ H(l = O) Het2 1766 —(CH₂)₅— SO₂CH₃ H(l = O) Het2 1767 H H PO(OCH₃)₂ H(l = O) Het2 1768 CH₃ CH₃ PO(OCH₃)₂ H(l = O) Het2 1769 CH₂CH₃ CH₂CH₃ PO(OCH₃)₂ H(l = O) Het2 1770 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₃)₂ H(l = O) Het2 1771 OCH₃ OCH₃ PO(OCH₃)₂ H(l = O) Het2 1772 OCH₂CH₃ OCH₂CH₃ PO(OCH₃)₂ H(l = O) Het2 1773 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₃)₂ H(l = O) Het2 1774 SCH₃ SCH₃ PO(OCH₃)₂ H(l = O) Het2 1775 SCH₂CH₃ SCH₂CH₃ PO(OCH₃)₂ H(l = O) Het2 1776 N(CH₃)₂ N(CH₃)₂ PO(OCH₃)₂ H(l = O) Het2 1777 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₃)₂ H(l = O) Het2 1778 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₃)₂ H(l = O) Het2 1779 O—(CH₂CH₂)—O PO(OCH₃)₂ H(l = O) Het2 1780 O—(CH₂CH₂CH₂)—O PO(OCH₃)₂ H(l = O) Het2 1781 S—(CH₂CH₂)—S PO(OCH₃)₂ H(l = O) Het2 1782 S—(CH₂CH₂CH₂)—S PO(OCH₃)₂ H(l = O) Het2 1783 —(CH₂)₄— PO(OCH₃)₂ H(l = O) Het2 1784 —(CH₂)₅— PO(OCH₃)₂ H(l = O) Het2 1785 H H PO(OCH₂CH₃)₂ H(l = O) Het2 1786 CH₃ CH₃ PO(OCH₂CH₃)₂ H(l = O) Het2 1787 CH₂CH₃ CH₂CH₃ PO(OCH₂CH₃)₂ H(l = O) Het2 1788 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₂CH₃)₂ H(l = O) Het2 1789 OCH₃ OCH₃ PO(OCH₂CH₃)₂ H(l = O) Het2 1790 OCH₂CH₃ OCH₂CH₃ PO(OCH₂CH₃)₂ H(l = O) Het2 1791 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₂CH₃)₂ H(l = O) Het2 1792 SCH₃ SCH₃ PO(OCH₂CH₃)₂ H(l = O) Het2 1793 SCH₂CH₃ SCH₂CH₃ PO(OCH₂CH₃)₂ H(l = O) Het2 1794 N(CH₃)₂ N(CH₃)₂ PO(OCH₂CH₃)₂ H(l = O) Het2 1795 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₂CH₃)₂ H(l = O) Het2 1796 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₂CH₃)₂ H(l = O) Het2 1797 O—(CH₂CH₂)—O PO(OCH₂CH₃)₂ H(l = O) Het2 1798 O—(CH₂CH₂CH₂)—O PO(OCH₂CH₃)₂ H(l = O) Het2 1799 S—(CH₂CH₂)—S PO(OCH₂CH₃)₂ H(l = O) Het2 1800 S—(CH₂CH₂CH₂)—S PO(OCH₂CH₃)₂ H(l = O) Het2 1801 —(CH₂)₄— PO(OCH₂CH₃)₂ H(l = O) Het2 1802 —(CH₂)₅— PO(OCH₂CH₃)₂ H(l = O) Het2 1803 H H PO(CH₃)₂ H(l = O) Het2 1804 CH₃ CH₃ PO(CH₃)₂ H(l = O) Het2 1805 CH₂CH₃ CH₂CH₃ PO(CH₃)₂ H(l = O) Het2 1806 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₃)₂ H(l = O) Het2 1807 OCH₃ OCH₃ PO(CH₃)₂ H(l = O) Het2 1808 OCH₂CH₃ OCH₂CH₃ PO(CH₃)₂ H(l = O) Het2 1809 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₃)₂ H(l = O) Het2 1810 SCH₃ SCH₃ PO(CH₃)₂ H(l = O) Het2 1811 SCH₂CH₃ SCH₂CH₃ PO(CH₃)₂ H(l = O) Het2 1812 N(CH₃)₂ N(CH₃)₂ PO(CH₃)₂ H(l = O) Het2 1813 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₃)₂ H(l = O) Het2 1814 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₃)₂ H(l = O) Het2 1815 O—(CH₂CH₂)—O PO(CH₃)₂ H(l = O) Het2 1816 O—(CH₂CH₂CH₂)—O PO(CH₃)₂ H(l = O) Het2 1817 S—(CH₂CH₂)—S PO(CH₃)₂ H(l = O) Het2 1818 S—(CH₂CH₂CH₂)—S PO(CH₃)₂ H(l = O) Het2 1819 —(CH₂)₄— PO(CH₃)₂ H(l = O) Het2 1820 —(CH₂)₅— PO(CH₃)₂ H(l = O) Het2 1821 H H PO(CH₂CH₃)₂ H(l = O) Het2 1822 CH₃ CH₃ PO(CH₂CH₃)₂ H(l = O) Het2 1823 CH₂CH₃ CH₂CH₃ PO(CH₂CH₃)₂ H(l = O) Het2 1824 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₂CH₃)₂ H(l = O) Het2 1825 OCH₃ OCH₃ PO(CH₂CH₃)₂ H(l = O) Het2 1826 OCH₂CH₃ OCH₂CH₃ PO(CH₂CH₃)₂ H(l = O) Het2 1827 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₂CH₃)₂ H(l = O) Het2 1828 SCH₃ SCH₃ PO(CH₂CH₃)₂ H(l = O) Het2 1829 SCH₂CH₃ SCH₂CH₃ PO(CH₂CH₃)₂ H(l = O) Het2 1830 N(CH₃)₂ N(CH₃)₂ PO(CH₂CH₃)₂ H(l = O) Het2 1831 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₂CH₃)₂ H(l = O) Het2 1832 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₂CH₃)₂ H(l = O) Het2 1833 O—(CH₂CH₂)—O PO(CH₂CH₃)₂ H(l = O) Het2 1834 O—(CH₂CH₂CH₂)—O PO(CH₂CH₃)₂ H(l = O) Het2 1835 S—(CH₂CH₂)—S PO(CH₂CH₃)₂ H(l = O) Het2 1836 S—(CH₂CH₂CH₂)—S PO(CH₂CH₃)₂ H(l = O) Het2 1837 —(CH₂)₄— PO(CH₂CH₃)₂ H(l = O) Het2 1838 —(CH₂)₅— PO(CH₂CH₃)₂ H(l = O) Het2 1839 H H H H(l = O) Het3 1840 CH₃ CH₃ H H(l = O) Het3 1841 CH₂CH₃ CH₂CH₃ H H(l = O) Het3 1842 CH₂CH₂CH₃ CH₂CH₂CH₃ H H(l = O) Het3 1843 OCH₃ OCH₃ H H(l = O) Het3 1844 OCH₂CH₃ OCH₂CH₃ H H(l = O) Het3 1845 OCH₂CH₂CH₃ OCH₂CH₂CH₃ H H(l = O) Het3 1846 SCH₃ SCH₃ H H(l = O) Het3 1847 SCH₂CH₃ SCH₂CH₃ H H(l = O) Het3 1848 N(CH₃)₂ N(CH₃)₂ H H(l = O) Het3 1849 N(CH₂CH₃)₂ N(CH₂CH₃)₂ H H(l = O) Het3 1850 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) H H(l = O) Het3 1851 O—(CH₂CH₂)—O H H(l = O) Het3 1852 O—(CH₂CH₂CH₂)—O H H(l = O) Het3 1853 S—(CH₂CH₂)—S H H(l = O) Het3 1854 S—(CH₂CH₂CH₂)—S H H(l = O) Het3 1855 —(CH₂)₄— H H(l = O) Het3 1856 —(CH₂)₅— H H(l = O) Het3 1857 H H NO₂ H(l = O) Het3 1858 CH₃ CH₃ NO₂ H(l = O) Het3 1859 CH₂CH₃ CH₂CH₃ NO₂ H(l = O) Het3 1860 CH₂CH₂CH₃ CH₂CH₂CH₃ NO₂ H(l = O) Het3 1861 OCH₃ OCH₃ NO₂ H(l = O) Het3 1862 OCH₂CH₃ OCH₂CH₃ NO₂ H(l = O) Het3 1863 OCH₂CH₂CH₃ OCH₂CH₂CH₃ NO₂ H(l = O) Het3 1864 SCH₃ SCH₃ NO₂ H(l = O) Het3 1865 SCH₂CH₃ SCH₂CH₃ NO₂ H(l = O) Het3 1866 N(CH₃)₂ N(CH₃)₂ NO₂ H(l = O) Het3 1867 N(CH₂CH₃)₂ N(CH₂CH₃)₂ NO₂ H(l = O) Het3 1868 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) NO₂ H(l = O) Het3 1869 O—(CH₂CH₂)—O NO₂ H(l = O) Het3 1870 O—(CH₂CH₂CH₂)—O NO₂ H(l = O) Het3 1871 S—(CH₂CH₂)—S NO₂ H(l = O) Het3 1872 S—(CH₂CH₂CH₂)—S NO₂ H(l = O) Het3 1873 —(CH₂)₄— NO₂ H(l = O) Het3 1874 —(CH₂)₅— NO₂ H(l = O) Het3 1875 H H CN H(l = O) Het3 1876 CH₃ CH₃ CN H(l = O) Het3 1877 CH₂CH₃ CH₂CH₃ CN H(l = O) Het3 1878 CH₂CH₂CH₃ CH₂CH₂CH₃ CN H(l = O) Het3 1879 OCH₃ OCH₃ CN H(l = O) Het3 1880 OCH₂CH₃ OCH₂CH₃ CN H(l = O) Het3 1881 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CN H(l = O) Het3 1882 SCH₃ SCH₃ CN H(l = O) Het3 1883 SCH₂CH₃ SCH₂CH₃ CN H(l = O) Het3 1884 N(CH₃)₂ N(CH₃)₂ CN H(l = O) Het3 1885 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CN H(l = O) Het3 1886 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CN H(l = O) Het3 1887 O—(CH₂CH₂)—O CN H(l = O) Het3 1888 O—(CH₂CH₂CH₂)—O CN H(l = O) Het3 1889 S—(CH₂CH₂)—S CN H(l = O) Het3 1890 S—(CH₂CH₂CH₂)—S CN H(l = O) Het3 1891 —(CH₂)₄— CN H(l = O) Het3 1892 —(CH₂)₅— CN H(l = O) Het3 1893 H H F H(l = O) Het3 1894 CH₃ CH₃ F H(l = O) Het3 1895 CH₂CH₃ CH₂CH₃ F H(l = O) Het3 1896 CH₂CH₂CH₃ CH₂CH₂CH₃ F H(l = O) Het3 1897 OCH₃ OCH₃ F H(l = O) Het3 1898 OCH₂CH₃ OCH₂CH₃ F H(l = O) Het3 1899 OCH₂CH₂CH₃ OCH₂CH₂CH₃ F H(l = O) Het3 1900 SCH₃ SCH₃ F H(l = O) Het3 1901 SCH₂CH₃ SCH₂CH₃ F H(l = O) Het3 1902 N(CH₃)₂ N(CH₃)₂ F H(l = O) Het3 1903 N(CH₂CH₃)₂ N(CH₂CH₃)₂ F H(l = O) Het3 1904 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) F H(l = O) Het3 1905 O—(CH₂CH₂)—O F H(l = O) Het3 1906 O—(CH₂CH₂CH₂)—O F H(l = O) Het3 1907 S—(CH₂CH₂)—S F H(l = O) Het3 1908 S—(CH₂CH₂CH₂)—S F H(l = O) Het3 1909 —(CH₂)₄— F H(l = O) Het3 1910 —(CH₂)₅— F H(l = O) Het3 1911 H H Cl H(l = O) Het3 1912 CH₃ CH₃ Cl H(l = O) Het3 1913 CH₂CH₃ CH₂CH₃ Cl H(l = O) Het3 1914 CH₂CH₂CH₃ CH₂CH₂CH₃ Cl H(l = O) Het3 1915 OCH₃ OCH₃ Cl H(l = O) Het3 1916 OCH₂CH₃ OCH₂CH₃ Cl H(l = O) Het3 1917 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Cl H(l = O) Het3 1918 SCH₃ SCH₃ Cl H(l = O) Het3 1919 SCH₂CH₃ SCH₂CH₃ Cl H(l = O) Het3 1920 N(CH₃)₂ N(CH₃)₂ Cl H(l = O) Het3 1921 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Cl H(l = O) Het3 1922 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Cl H(l = O) Het3 1923 O—(CH₂CH₂)—O Cl H(l = O) Het3 1924 O—(CH₂CH₂CH₂)—O Cl H(l = O) Het3 1925 S—(CH₂CH₂)—S Cl H(l = O) Het3 1926 S—(CH₂CH₂CH₂)—S Cl H(l = O) Het3 1927 —(CH₂)₄— Cl H(l = O) Het3 1928 —(CH₂)₅— Cl H(l = O) Het3 1929 H H Br H(l = O) Het3 1930 CH₃ CH₃ Br H(l = O) Het3 1931 CH₂CH₃ CH₂CH₃ Br H(l = O) Het3 1932 CH₂CH₂CH₃ CH₂CH₂CH₃ Br H(l = O) Het3 1933 OCH₃ OCH₃ Br H(l = O) Het3 1934 OCH₂CH₃ OCH₂CH₃ Br H(l = O) Het3 1935 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Br H(l = O) Het3 1936 SCH₃ SCH₃ Br H(l = O) Het3 1937 SCH₂CH₃ SCH₂CH₃ Br H(l = O) Het3 1938 N(CH₃)₂ N(CH₃)₂ Br H(l = O) Het3 1939 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Br H(l = O) Het3 1940 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Br H(l = O) Het3 1941 O—(CH₂CH₂)—O Br H(l = O) Het3 1942 O—(CH₂CH₂CH₂)—O Br H(l = O) Het3 1943 S—(CH₂CH₂)—S Br H(l = O) Het3 1944 S—(CH₂CH₂CH₂)—S Br H(l = O) Het3 1945 —(CH₂)₄— Br H(l = O) Het3 1946 —(CH₂)₅— Br H(l = O) Het3 1947 H H CH₃ H(l = O) Het3 1948 CH₃ CH₃ CH₃ H(l = O) Het3 1949 CH₂CH₃ CH₂CH₃ CH₃ H(l = O) Het3 1950 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₃ H(l = O) Het3 1951 OCH₃ OCH₃ CH₃ H(l = O) Het3 1952 OCH₂CH₃ OCH₂CH₃ CH₃ H(l = O) Het3 1953 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₃ H(l = O) Het3 1954 SCH₃ SCH₃ CH₃ H(l = O) Het3 1955 SCH₂CH₃ SCH₂CH₃ CH₃ H(l = O) Het3 1956 N(CH₃)₂ N(CH₃)₂ CH₃ H(l = O) Het3 1957 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₃ H(l = O) Het3 1958 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₃ H(l = O) Het3 1959 O—(CH₂CH₂)—O CH₃ H(l = O) Het3 1960 O—(CH₂CH₂CH₂)—O CH₃ H(l = O) Het3 1961 S—(CH₂CH₂)—S CH₃ H(l = O) Het3 1962 S—(CH₂CH₂CH₂)—S CH₃ H(l = O) Het3 1963 —(CH₂)₄— CH₃ H(l = O) Het3 1964 —(CH₂)₅— CH₃ H(l = O) Het3 1965 H H CH₂CH₃ H(l = O) Het3 1966 CH₃ CH₃ CH₂CH₃ H(l = O) Het3 1967 CH₂CH₃ CH₂CH₃ CH₂CH₃ H(l = O) Het3 1968 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₂CH₃ H(l = O) Het3 1969 OCH₃ OCH₃ CH₂CH₃ H(l = O) Het3 1970 OCH₂CH₃ OCH₂CH₃ CH₂CH₃ H(l = O) Het3 1971 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₂CH₃ H(l = O) Het3 1972 SCH₃ SCH₃ CH₂CH₃ H(l = O) Het3 1973 SCH₂CH₃ SCH₂CH₃ CH₂CH₃ H(l = O) Het3 1974 N(CH₃)₂ N(CH₃)₂ CH₂CH₃ H(l = O) Het3 1975 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₂CH₃ H(l = O) Het3 1976 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₂CH₃ H(l = O) Het3 1977 O—(CH₂CH₂)—O CH₂CH₃ H(l = O) Het3 1978 O—(CH₂CH₂CH₂)—O CH₂CH₃ H(l = O) Het3 1979 S—(CH₂CH₂)—S CH₂CH₃ H(l = O) Het3 1980 S—(CH₂CH₂CH₂)—S CH₂CH₃ H(l = O) Het3 1981 —(CH₂)₄— CH₂CH₃ H(l = O) Het3 1982 —(CH₂)₅— CH₂CH₃ H(l = O) Het3 1983 H H CF₃ H(l = O) Het3 1984 CH₃ CH₃ CF₃ H(l = O) Het3 1985 CH₂CH₃ CH₂CH₃ CF₃ H(l = O) Het3 1986 CH₂CH₂CH₃ CH₂CH₂CH₃ CF₃ H(l = O) Het3 1987 OCH₃ OCH₃ CF₃ H(l = O) Het3 1988 OCH₂CH₃ OCH₂CH₃ CF₃ H(l = O) Het3 1989 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CF₃ H(l = O) Het3 1990 SCH₃ SCH₃ CF₃ H(l = O) Het3 1991 SCH₂CH₃ SCH₂CH₃ CF₃ H(l = O) Het3 1992 N(CH₃)₂ N(CH₃)₂ CF₃ H(l = O) Het3 1993 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CF₃ H(l = O) Het3 1994 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CF₃ H(l = O) Het3 1995 O—(CH₂CH₂)—O CF₃ H(l = O) Het3 1996 O—(CH₂CH₂CH₂)—O CF₃ H(l = O) Het3 1997 S—(CH₂CH₂)—S CF₃ H(l = O) Het3 1998 S—(CH₂CH₂CH₂)—S CF₃ H(l = O) Het3 1999 —(CH₂)₄— CF₃ H(l = O) Het3 2000 —(CH₂)₅— CF₃ H(l = O) Het3 2001 H H OCH₃ H(l = O) Het3 2002 CH₃ CH₃ OCH₃ H(l = O) Het3 2003 CH₂CH₃ CH₂CH₃ OCH₃ H(l = O) Het3 2004 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₃ H(l = O) Het3 2005 OCH₃ OCH₃ OCH₃ H(l = O) Het3 2006 OCH₂CH₃ OCH₂CH₃ OCH₃ H(l = O) Het3 2007 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₃ H(l = O) Het3 2008 SCH₃ SCH₃ OCH₃ H(l = O) Het3 2009 SCH₂CH₃ SCH₂CH₃ OCH₃ H(l = O) Het3 2010 N(CH₃)₂ N(CH₃)₂ OCH₃ H(l = O) Het3 2011 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₃ H(l = O) Het3 2012 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₃ H(l = O) Het3 2013 O—(CH₂CH₂)—O OCH₃ H(l = O) Het3 2014 O—(CH₂CH₂CH₂)—O OCH₃ H(l = O) Het3 2015 S—(CH₂CH₂)—S OCH₃ H(l = O) Het3 2016 S—(CH₂CH₂CH₂)—S OCH₃ H(l = O) Het3 2017 —(CH₂)₄— OCH₃ H(l = O) Het3 2018 —(CH₂)₅— OCH₃ H(l = O) Het3 2019 H H OCH₂CH₃ H(l = O) Het3 2020 CH₃ CH₃ OCH₂CH₃ H(l = O) Het3 2021 CH₂CH₃ CH₂CH₃ OCH₂CH₃ H(l = O) Het3 2022 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₂CH₃ H(l = O) Het3 2023 OCH₃ OCH₃ OCH₂CH₃ H(l = O) Het3 2024 OCH₂CH₃ OCH₂CH₃ OCH₂CH₃ H(l = O) Het3 2025 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₂CH₃ H(l = O) Het3 2026 SCH₃ SCH₃ OCH₂CH₃ H(l = O) Het3 2027 SCH₂CH₃ SCH₂CH₃ OCH₂CH₃ H(l = O) Het3 2028 N(CH₃)₂ N(CH₃)₂ OCH₂CH₃ H(l = O) Het3 2029 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₂CH₃ H(l = O) Het3 2030 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₂CH₃ H(l = O) Het3 2031 O—(CH₂CH₂)—O OCH₂CH₃ H(l = O) Het3 2032 O—(CH₂CH₂CH₂)—O OCH₂CH₃ H(l = O) Het3 2033 S—(CH₂CH₂)—S OCH₂CH₃ H(l = O) Het3 2034 S—(CH₂CH₂CH₂)—S OCH₂CH₃ H(l = O) Het3 2035 —(CH₂)₄— OCH₂CH₃ H(l = O) Het3 2036 —(CH₂)₅— OCH₂CH₃ H(l = O) Het3 2037 H H SCH₃ H(l = O) Het3 2038 CH₃ CH₃ SCH₃ H(l = O) Het3 2039 CH₂CH₃ CH₂CH₃ SCH₃ H(l = O) Het3 2040 CH₂CH₂CH₃ CH₂CH₂CH₃ SCH₃ H(l = O) Het3 2041 OCH₃ OCH₃ SCH₃ H(l = O) Het3 2042 OCH₂CH₃ OCH₂CH₃ SCH₃ H(l = O) Het3 2043 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SCH₃ H(l = O) Het3 2044 SCH₃ SCH₃ SCH₃ H(l = O) Het3 2045 SCH₂CH₃ SCH₂CH₃ SCH₃ H(l = O) Het3 2046 N(CH₃)₂ N(CH₃)₂ SCH₃ H(l = O) Het3 2047 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SCH₃ H(l = O) Het3 2048 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SCH₃ H(l = O) Het3 2049 O—(CH₂CH₂)—O SCH₃ H(l = O) Het3 2050 O—(CH₂CH₂CH₂)—O SCH₃ H(l = O) Het3 2051 S—(CH₂CH₂)—S SCH₃ H(l = O) Het3 2052 S—(CH₂CH₂CH₂)—S SCH₃ H(l = O) Het3 2053 —(CH₂)₄— SCH₃ H(l = O) Het3 2054 —(CH₂)₅— SCH₃ H(l = O) Het3 2055 H H SO₂CH₃ H(l = O) Het3 2056 CH₃ CH₃ SO₂CH₃ H(l = O) Het3 2057 CH₂CH₃ CH₂CH₃ SO₂CH₃ H(l = O) Het3 2058 CH₂CH₂CH₃ CH₂CH₂CH₃ SO₂CH₃ H(l = O) Het3 2059 OCH₃ OCH₃ SO₂CH₃ H(l = O) Het3 2060 OCH₂CH₃ OCH₂CH₃ SO₂CH₃ H(l = O) Het3 2061 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SO₂CH₃ H(l = O) Het3 2062 SCH₃ SCH₃ SO₂CH₃ H(l = O) Het3 2063 SCH₂CH₃ SCH₂CH₃ SO₂CH₃ H(l = O) Het3 2064 N(CH₃)₂ N(CH₃)₂ SO₂CH₃ H(l = O) Het3 2065 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SO₂CH₃ H(l = O) Het3 2066 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SO₂CH₃ H(l = O) Het3 2067 O—(CH₂CH₂)—O SO₂CH₃ H(l = O) Het3 2068 O—(CH₂CH₂CH₂)—O SO₂CH₃ H(l = O) Het3 2069 S—(CH₂CH₂)—S SO₂CH₃ H(l = O) Het3 2070 S—(CH₂CH₂CH₂)—S SO₂CH₃ H(l = O) Het3 2071 —(CH₂)₄— SO₂CH₃ H(l = O) Het3 2072 —(CH₂)₅— SO₂CH₃ H(l = O) Het3 2073 H H PO(OCH₃)₂ H(l = O) Het3 2074 CH₃ CH₃ PO(OCH₃)₂ H(l = O) Het3 2075 CH₂CH₃ CH₂CH₃ PO(OCH₃)₂ H(l = O) Het3 2076 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₃)₂ H(l = O) Het3 2077 OCH₃ OCH₃ PO(OCH₃)₂ H(l = O) Het3 2078 OCH₂CH₃ OCH₂CH₃ PO(OCH₃)₂ H(l = O) Het3 2079 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₃)₂ H(l = O) Het3 2080 SCH₃ SCH₃ PO(OCH₃)₂ H(l = O) Het3 2081 SCH₂CH₃ SCH₂CH₃ PO(OCH₃)₂ H(l = O) Het3 2082 N(CH₃)₂ N(CH₃)₂ PO(OCH₃)₂ H(l = O) Het3 2083 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₃)₂ H(l = O) Het3 2084 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₃)₂ H(l = O) Het3 2085 O—(CH₂CH₂)—O PO(OCH₃)₂ H(l = O) Het3 2086 O—(CH₂CH₂CH₂)—O PO(OCH₃)₂ H(l = O) Het3 2087 S—(CH₂CH₂)—S PO(OCH₃)₂ H(l = O) Het3 2088 S—(CH₂CH₂CH₂)—S PO(OCH₃)₂ H(l = O) Het3 2089 —(CH₂)₄— PO(OCH₃)₂ H(l = O) Het3 2090 —(CH₂)₅— PO(OCH₃)₂ H(l = O) Het3 2091 H H PO(OCH₂CH₃)₂ H(l = O) Het3 2092 CH₃ CH₃ PO(OCH₂CH₃)₂ H(l = O) Het3 2093 CH₂CH₃ CH₂CH₃ PO(OCH₂CH₃)₂ H(l = O) Het3 2094 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₂CH₃)₂ H(l = O) Het3 2095 OCH₃ OCH₃ PO(OCH₂CH₃)₂ H(l = O) Het3 2096 OCH₂CH₃ OCH₂CH₃ PO(OCH₂CH₃)₂ H(l = O) Het3 2097 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₂CH₃)₂ H(l = O) Het3 2098 SCH₃ SCH₃ PO(OCH₂CH₃)₂ H(l = O) Het3 2099 SCH₂CH₃ SCH₂CH₃ PO(OCH₂CH₃)₂ H(l = O) Het3 2100 N(CH₃)₂ N(CH₃)₂ PO(OCH₂CH₃)₂ H(l = O) Het3 2101 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₂CH₃)₂ H(l = O) Het3 2102 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₂CH₃)₂ H(l = O) Het3 2103 O—(CH₂CH₂)—O PO(OCH₂CH₃)₂ H(l = O) Het3 2104 O—(CH₂CH₂CH₂)—O PO(OCH₂CH₃)₂ H(l = O) Het3 2105 S—(CH₂CH₂)—S PO(OCH₂CH₃)₂ H(l = O) Het3 2106 S—(CH₂CH₂CH₂)—S PO(OCH₂CH₃)₂ H(l = O) Het3 2107 —(CH₂)₄— PO(OCH₂CH₃)₂ H(l = O) Het3 2108 —(CH₂)₅— PO(OCH₂CH₃)₂ H(l = O) Het3 2109 H H PO(CH₃)₂ H(l = O) Het3 2110 CH₃ CH₃ PO(CH₃)₂ H(l = O) Het3 2111 CH₂CH₃ CH₂CH₃ PO(CH₃)₂ H(l = O) Het3 2112 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₃)₂ H(l = O) Het3 2113 OCH₃ OCH₃ PO(CH₃)₂ H(l = O) Het3 2114 OCH₂CH₃ OCH₂CH₃ PO(CH₃)₂ H(l = O) Het3 2115 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₃)₂ H(l = O) Het3 2116 SCH₃ SCH₃ PO(CH₃)₂ H(l = O) Het3 2117 SCH₂CH₃ SCH₂CH₃ PO(CH₃)₂ H(l = O) Het3 2118 N(CH₃)₂ N(CH₃)₂ PO(CH₃)₂ H(l = O) Het3 2119 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₃)₂ H(l = O) Het3 2120 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₃)₂ H(l = O) Het3 2121 O—(CH₂CH₂)—O PO(CH₃)₂ H(l = O) Het3 2122 O—(CH₂CH₂CH₂)—O PO(CH₃)₂ H(l = O) Het3 2123 S—(CH₂CH₂)—S PO(CH₃)₂ H(l = O) Het3 2124 S—(CH₂CH₂CH₂)—S PO(CH₃)₂ H(l = O) Het3 2125 —(CH₂)₄— PO(CH₃)₂ H(l = O) Het3 2126 —(CH₂)₅— PO(CH₃)₂ H(l = O) Het3 2127 H H PO(CH₂CH₃)₂ H(l = O) Het3 2128 CH₃ CH₃ PO(CH₂CH₃)₂ H(l = O) Het3 2129 CH₂CH₃ CH₂CH₃ PO(CH₂CH₃)₂ H(l = O) Het3 2130 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₂CH₃)₂ H(l = O) Het3 2131 OCH₃ OCH₃ PO(CH₂CH₃)₂ H(l = O) Het3 2132 OCH₂CH₃ OCH₂CH₃ PO(CH₂CH₃)₂ H(l = O) Het3 2133 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₂CH₃)₂ H(l = O) Het3 2134 SCH₃ SCH₃ PO(CH₂CH₃)₂ H(l = O) Het3 2135 SCH₂CH₃ SCH₂CH₃ PO(CH₂CH₃)₂ H(l = O) Het3 2136 N(CH₃)₂ N(CH₃)₂ PO(CH₂CH₃)₂ H(l = O) Het3 2137 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₂CH₃)₂ H(l = O) Het3 2138 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₂CH₃)₂ H(l = O) Het3 2139 O—(CH₂CH₂)—O PO(CH₂CH₃)₂ H(l = O) Het3 2140 O—(CH₂CH₂CH₂)—O PO(CH₂CH₃)₂ H(l = O) Het3 2141 S—(CH₂CH₂)—S PO(CH₂CH₃)₂ H(l = O) Het3 2142 S—(CH₂CH₂CH₂)—S PO(CH₂CH₃)₂ H(l = O) Het3 2143 —(CH₂)₄— PO(CH₂CH₃)₂ H(l = O) Het3 2144 —(CH₂)₅— PO(CH₂CH₃)₂ H(l = O) Het3 2145 H H H CH₃ OH 2146 CH₃ CH₃ H CH₃ OH 2147 CH₂CH₃ CH₂CH₃ H CH₃ OH 2148 CH₂CH₂CH₃ CH₂CH₂CH₃ H CH₃ OH 2149 OCH₃ OCH₃ H CH₃ OH 2150 OCH₂CH₃ OCH₂CH₃ H CH₃ OH 2151 OCH₂CH₂CH₃ OCH₂CH₂CH₃ H CH₃ OH 2152 SCH₃ SCH₃ H CH₃ OH 2153 SCH₂CH₃ SCH₂CH₃ H CH₃ OH 2154 N(CH₃)₂ N(CH₃)₂ H CH₃ OH 2155 N(CH₂CH₃)₂ N(CH₂CH₃)₂ H CH₃ OH 2156 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) H CH₃ OH 2157 O—(CH₂CH₂)—O H CH₃ OH 2158 O—(CH₂CH₂CH₂)—O H CH₃ OH 2159 S—(CH₂CH₂)—S H CH₃ OH 2160 S—(CH₂CH₂CH₂)—S H CH₃ OH 2161 —(CH₂)₄— H CH₃ OH 2162 —(CH₂)₅— H CH₃ OH 2163 H H NO₂ CH₃ OH 2164 CH₃ CH₃ NO₂ CH₃ OH 2165 CH₂CH₃ CH₂CH₃ NO₂ CH₃ OH 2166 CH₂CH₂CH₃ CH₂CH₂CH₃ NO₂ CH₃ OH 2167 OCH₃ OCH₃ NO₂ CH₃ OH 2168 OCH₂CH₃ OCH₂CH₃ NO₂ CH₃ OH 2169 OCH₂CH₂CH₃ OCH₂CH₂CH₃ NO₂ CH₃ OH 2170 SCH₃ SCH₃ NO₂ CH₃ OH 2171 SCH₂CH₃ SCH₂CH₃ NO₂ CH₃ OH 2172 N(CH₃)₂ N(CH₃)₂ NO₂ CH₃ OH 2173 N(CH₂CH₃)₂ N(CH₂CH₃)₂ NO₂ CH₃ OH 2174 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) NO₂ CH₃ OH 2175 O—(CH₂CH₂)—O NO₂ CH₃ OH 2176 O—(CH₂CH₂CH₂)—O NO₂ CH₃ OH 2177 S—(CH₂CH₂)—S NO₂ CH₃ OH 2178 S—(CH₂CH₂CH₂)—S NO₂ CH₃ OH 2179 —(CH₂)₄— NO₂ CH₃ OH 2180 —(CH₂)₅— NO₂ CH₃ OH 2181 H H CN CH₃ OH 2182 CH₃ CH₃ CN CH₃ OH 2183 CH₂CH₃ CH₂CH₃ CN CH₃ OH 2184 CH₂CH₂CH₃ CH₂CH₂CH₃ CN CH₃ OH 2185 OCH₃ OCH₃ CN CH₃ OH 2186 OCH₂CH₃ OCH₂CH₃ CN CH₃ OH 2187 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CN CH₃ OH 2188 SCH₃ SCH₃ CN CH₃ OH 2189 SCH₂CH₃ SCH₂CH₃ CN CH₃ OH 2190 N(CH₃)₂ N(CH₃)₂ CN CH₃ OH 2191 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CN CH₃ OH 2192 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CN CH₃ OH 2193 O—(CH₂CH₂)—O CN CH₃ OH 2194 O—(CH₂CH₂CH₂)—O CN CH₃ OH 2195 S—(CH₂CH₂)—S CN CH₃ OH 2196 S—(CH₂CH₂CH₂)—S CN CH₃ OH 2197 —(CH₂)₄— CN CH₃ OH 2198 —(CH₂)₅— CN CH₃ OH 2199 H H F CH₃ OH 2200 CH₃ CH₃ F CH₃ OH 2201 CH₂CH₃ CH₂CH₃ F CH₃ OH 2202 CH₂CH₂CH₃ CH₂CH₂CH₃ F CH₃ OH 2203 OCH₃ OCH₃ F CH₃ OH 2204 OCH₂CH₃ OCH₂CH₃ F CH₃ OH 2205 OCH₂CH₂CH₃ OCH₂CH₂CH₃ F CH₃ OH 2206 SCH₃ SCH₃ F CH₃ OH 2207 SCH₂CH₃ SCH₂CH₃ F CH₃ OH 2208 N(CH₃)₂ N(CH₃)₂ F CH₃ OH 2209 N(CH₂CH₃)₂ N(CH₂CH₃)₂ F CH₃ OH 2210 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) F CH₃ OH 2211 O—(CH₂CH₂)—O F CH₃ OH 2212 O—(CH₂CH₂CH₂)—O F CH₃ OH 2213 S—(CH₂CH₂)—S F CH₃ OH 2214 S—(CH₂CH₂CH₂)—S F CH₃ OH 2215 —(CH₂)₄— F CH₃ OH 2216 —(CH₂)₅— F CH₃ OH 2217 H H Cl CH₃ OH 2218 CH₃ CH₃ Cl CH₃ OH 2219 CH₂CH₃ CH₂CH₃ Cl CH₃ OH 2220 CH₂CH₂CH₃ CH₂CH₂CH₃ Cl CH₃ OH 2221 OCH₃ OCH₃ Cl CH₃ OH 2222 OCH₂CH₃ OCH₂CH₃ Cl CH₃ OH 2223 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Cl CH₃ OH 2224 SCH₃ SCH₃ Cl CH₃ OH 2225 SCH₂CH₃ SCH₂CH₃ Cl CH₃ OH 2226 N(CH₃)₂ N(CH₃)₂ Cl CH₃ OH 2227 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Cl CH₃ OH 2228 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Cl CH₃ OH 2229 O—(CH₂CH₂)—O Cl CH₃ OH 2230 O—(CH₂CH₂CH₂)—O Cl CH₃ OH 2231 S—(CH₂CH₂)—S Cl CH₃ OH 2232 S—(CH₂CH₂CH₂)—S Cl CH₃ OH 2233 —(CH₂)₄— Cl CH₃ OH 2234 —(CH₂)₅— Cl CH₃ OH 2235 H H Br CH₃ OH 2236 CH₃ CH₃ Br CH₃ OH 2237 CH₂CH₃ CH₂CH₃ Br CH₃ OH 2238 CH₂CH₂CH₃ CH₂CH₂CH₃ Br CH₃ OH 2239 OCH₃ OCH₃ Br CH₃ OH 2240 OCH₂CH₃ OCH₂CH₃ Br CH₃ OH 2241 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Br CH₃ OH 2242 SCH₃ SCH₃ Br CH₃ OH 2243 SCH₂CH₃ SCH₂CH₃ Br CH₃ OH 2244 N(CH₃)₂ N(CH₃)₂ Br CH₃ OH 2245 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Br CH₃ OH 2246 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Br CH₃ OH 2247 O—(CH₂CH₂)—O Br CH₃ OH 2248 O—(CH₂CH₂CH₂)—O Br CH₃ OH 2249 S—(CH₂CH₂)—S Br CH₃ OH 2250 S—(CH₂CH₂CH₂)—S Br CH₃ OH 2251 —(CH₂)₄— Br CH₃ OH 2252 —(CH₂)₅— Br CH₃ OH 2253 H H CH₃ CH₃ OH 2254 CH₃ CH₃ CH₃ CH₃ OH 2255 CH₂CH₃ CH₂CH₃ CH₃ CH₃ OH 2256 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₃ CH₃ OH 2257 OCH₃ OCH₃ CH₃ CH₃ OH 2258 OCH₂CH₃ OCH₂CH₃ CH₃ CH₃ OH 2259 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₃ CH₃ OH 2260 SCH₃ SCH₃ CH₃ CH₃ OH 2261 SCH₂CH₃ SCH₂CH₃ CH₃ CH₃ OH 2262 N(CH₃)₂ N(CH₃)₂ CH₃ CH₃ OH 2263 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₃ CH₃ OH 2264 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₃ CH₃ OH 2265 O—(CH₂CH₂)—O CH₃ CH₃ OH 2266 O—(CH₂CH₂CH₂)—O CH₃ CH₃ OH 2267 S—(CH₂CH₂)—S CH₃ CH₃ OH 2268 S—(CH₂CH₂CH₂)—S CH₃ CH₃ OH 2269 —(CH₂)₄— CH₃ CH₃ OH 2270 —(CH₂)₅— CH₃ CH₃ OH 2271 H H CH₂CH₃ CH₃ OH 2272 CH₃ CH₃ CH₂CH₃ CH₃ OH 2273 CH₂CH₃ CH₂CH₃ CH₂CH₃ CH₃ OH 2274 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₂CH₃ CH₃ OH 2275 OCH₃ OCH₃ CH₂CH₃ CH₃ OH 2276 OCH₂CH₃ OCH₂CH₃ CH₂CH₃ CH₃ OH 2277 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₂CH₃ CH₃ OH 2278 SCH₃ SCH₃ CH₂CH₃ CH₃ OH 2279 SCH₂CH₃ SCH₂CH₃ CH₂CH₃ CH₃ OH 2280 N(CH₃)₂ N(CH₃)₂ CH₂CH₃ CH₃ OH 2281 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₂CH₃ CH₃ OH 2282 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₂CH₃ CH₃ OH 2283 O—(CH₂CH₂)—O CH₂CH₃ CH₃ OH 2284 O—(CH₂CH₂CH₂)—O CH₂CH₃ CH₃ OH 2285 S—(CH₂CH₂)—S CH₂CH₃ CH₃ OH 2286 S—(CH₂CH₂CH₂)—S CH₂CH₃ CH₃ OH 2287 —(CH₂)₄— CH₂CH₃ CH₃ OH 2288 —(CH₂)₅— CH₂CH₃ CH₃ OH 2289 H H CF₃ CH₃ OH 2290 CH₃ CH₃ CF₃ CH₃ OH 2291 CH₂CH₃ CH₂CH₃ CF₃ CH₃ OH 2292 CH₂CH₂CH₃ CH₂CH₂CH₃ CF₃ CH₃ OH 2293 OCH₃ OCH₃ CF₃ CH₃ OH 2294 OCH₂CH₃ OCH₂CH₃ CF₃ CH₃ OH 2295 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CF₃ CH₃ OH 2296 SCH₃ SCH₃ CF₃ CH₃ OH 2297 SCH₂CH₃ SCH₂CH₃ CF₃ CH₃ OH 2298 N(CH₃)₂ N(CH₃)₂ CF₃ CH₃ OH 2299 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CF₃ CH₃ OH 2300 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CF₃ CH₃ OH 2301 O—(CH₂CH₂)—O CF₃ CH₃ OH 2302 O—(CH₂CH₂CH₂)—O CF₃ CH₃ OH 2303 S—(CH₂CH₂)—S CF₃ CH₃ OH 2304 S—(CH₂CH₂CH₂)—S CF₃ CH₃ OH 2305 —(CH₂)₄— CF₃ CH₃ OH 2306 —(CH₂)₅— CF₃ CH₃ OH 2307 H H OCH₃ CH₃ OH 2308 CH₃ CH₃ OCH₃ CH₃ OH 2309 CH₂CH₃ CH₂CH₃ OCH₃ CH₃ OH 2310 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₃ CH₃ OH 2311 OCH₃ OCH₃ OCH₃ CH₃ OH 2312 OCH₂CH₃ OCH₂CH₃ OCH₃ CH₃ OH 2313 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₃ CH₃ OH 2314 SCH₃ SCH₃ OCH₃ CH₃ OH 2315 SCH₂CH₃ SCH₂CH₃ OCH₃ CH₃ OH 2316 N(CH₃)₂ N(CH₃)₂ OCH₃ CH₃ OH 2317 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₃ CH₃ OH 2318 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₃ CH₃ OH 2319 O—(CH₂CH₂)—O OCH₃ CH₃ OH 2320 O—(CH₂CH₂CH₂)—O OCH₃ CH₃ OH 2321 S—(CH₂CH₂)—S OCH₃ CH₃ OH 2322 S—(CH₂CH₂CH₂)—S OCH₃ CH₃ OH 2323 —(CH₂)₄— OCH₃ CH₃ OH 2324 —(CH₂)₅— OCH₃ CH₃ OH 2325 H H OCH₂CH₃ CH₃ OH 2326 CH₃ CH₃ OCH₂CH₃ CH₃ OH 2327 CH₂CH₃ CH₂CH₃ OCH₂CH₃ CH₃ OH 2328 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₂CH₃ CH₃ OH 2329 OCH₃ OCH₃ OCH₂CH₃ CH₃ OH 2330 OCH₂CH₃ OCH₂CH₃ OCH₂CH₃ CH₃ OH 2331 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₂CH₃ CH₃ OH 2332 SCH₃ SCH₃ OCH₂CH₃ CH₃ OH 2333 SCH₂CH₃ SCH₂CH₃ OCH₂CH₃ CH₃ OH 2334 N(CH₃)₂ N(CH₃)₂ OCH₂CH₃ CH₃ OH 2335 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₂CH₃ CH₃ OH 2336 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₂CH₃ CH₃ OH 2337 O—(CH₂CH₂)—O OCH₂CH₃ CH₃ OH 2338 O—(CH₂CH₂CH₂)—O OCH₂CH₃ CH₃ OH 2339 S—(CH₂CH₂)—S OCH₂CH₃ CH₃ OH 2340 S—(CH₂CH₂CH₂)—S OCH₂CH₃ CH₃ OH 2341 —(CH₂)₄— OCH₂CH₃ CH₃ OH 2342 —(CH₂)₅— OCH₂CH₃ CH₃ OH 2343 H H SCH₃ CH₃ OH 2344 CH₃ CH₃ SCH₃ CH₃ OH 2345 CH₂CH₃ CH₂CH₃ SCH₃ CH₃ OH 2346 CH₂CH₂CH₃ CH₂CH₂CH₃ SCH₃ CH₃ OH 2347 OCH₃ OCH₃ SCH₃ CH₃ OH 2348 OCH₂CH₃ OCH₂CH₃ SCH₃ CH₃ OH 2349 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SCH₃ CH₃ OH 2350 SCH₃ SCH₃ SCH₃ CH₃ OH 2351 SCH₂CH₃ SCH₂CH₃ SCH₃ CH₃ OH 2352 N(CH₃)₂ N(CH₃)₂ SCH₃ CH₃ OH 2353 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SCH₃ CH₃ OH 2354 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SCH₃ CH₃ OH 2355 O—(CH₂CH₂)—O SCH₃ CH₃ OH 2356 O—(CH₂CH₂CH₂)—O SCH₃ CH₃ OH 2357 S—(CH₂CH₂)—S SCH₃ CH₃ OH 2358 S—(CH₂CH₂CH₂)—S SCH₃ CH₃ OH 2359 —(CH₂)₄— SCH₃ CH₃ OH 2360 —(CH₂)₅— SCH₃ CH₃ OH 2361 H H SO₂CH₃ CH₃ OH 2362 CH₃ CH₃ SO₂CH₃ CH₃ OH 2363 CH₂CH₃ CH₂CH₃ SO₂CH₃ CH₃ OH 2364 CH₂CH₂CH₃ CH₂CH₂CH₃ SO₂CH₃ CH₃ OH 2365 OCH₃ OCH₃ SO₂CH₃ CH₃ OH 2366 OCH₂CH₃ OCH₂CH₃ SO₂CH₃ CH₃ OH 2367 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SO₂CH₃ CH₃ OH 2368 SCH₃ SCH₃ SO₂CH₃ CH₃ OH 2369 SCH₂CH₃ SCH₂CH₃ SO₂CH₃ CH₃ OH 2370 N(CH₃)₂ N(CH₃)₂ SO₂CH₃ CH₃ OH 2371 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SO₂CH₃ CH₃ OH 2372 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SO₂CH₃ CH₃ OH 2373 O—(CH₂CH₂)—O SO₂CH₃ CH₃ OH 2374 O—(CH₂CH₂CH₂)—O SO₂CH₃ CH₃ OH 2375 S—(CH₂CH₂)—S SO₂CH₃ CH₃ OH 2376 S—(CH₂CH₂CH₂)—S SO₂CH₃ CH₃ OH 2377 —(CH₂)₄— SO₂CH₃ CH₃ OH 2378 —(CH₂)₅— SO₂CH₃ CH₃ OH 2379 H H PO(OCH₃)₂ CH₃ OH 2380 CH₃ CH₃ PO(OCH₃)₂ CH₃ OH 2381 CH₂CH₃ CH₂CH₃ PO(OCH₃)₂ CH₃ OH 2382 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₃)₂ CH₃ OH 2383 OCH₃ OCH₃ PO(OCH₃)₂ CH₃ OH 2384 OCH₂CH₃ OCH₂CH₃ PO(OCH₃)₂ CH₃ OH 2385 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₃)₂ CH₃ OH 2386 SCH₃ SCH₃ PO(OCH₃)₂ CH₃ OH 2387 SCH₂CH₃ SCH₂CH₃ PO(OCH₃)₂ CH₃ OH 2388 N(CH₃)₂ N(CH₃)₂ PO(OCH₃)₂ CH₃ OH 2389 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₃)₂ CH₃ OH 2390 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₃)₂ CH₃ OH 2391 O—(CH₂CH₂)—O PO(OCH₃)₂ CH₃ OH 2392 O—(CH₂CH₂CH₂)—O PO(OCH₃)₂ CH₃ OH 2393 S—(CH₂CH₂)—S PO(OCH₃)₂ CH₃ OH 2394 S—(CH₂CH₂CH₂)—S PO(OCH₃)₂ CH₃ OH 2395 —(CH₂)₄— PO(OCH₃)₂ CH₃ OH 2396 —(CH₂)₅— PO(OCH₃)₂ CH₃ OH 2397 H H PO(OCH₂CH₃)₂ CH₃ OH 2398 CH₃ CH₃ PO(OCH₂CH₃)₂ CH₃ OH 2399 CH₂CH₃ CH₂CH₃ PO(OCH₂CH₃)₂ CH₃ OH 2400 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₂CH₃)₂ CH₃ OH 2401 OCH₃ OCH₃ PO(OCH₂CH₃)₂ CH₃ OH 2402 OCH₂CH₃ OCH₂CH₃ PO(OCH₂CH₃)₂ CH₃ OH 2403 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₂CH₃)₂ CH₃ OH 2404 SCH₃ SCH₃ PO(OCH₂CH₃)₂ CH₃ OH 2405 SCH₂CH₃ SCH₂CH₃ PO(OCH₂CH₃)₂ CH₃ OH 2406 N(CH₃)₂ N(CH₃)₂ PO(OCH₂CH₃)₂ CH₃ OH 2407 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₂CH₃)₂ CH₃ OH 2408 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₂CH₃)₂ CH₃ OH 2409 O—(CH₂CH₂)—O PO(OCH₂CH₃)₂ CH₃ OH 2410 O—(CH₂CH₂CH₂)—O PO(OCH₂CH₃)₂ CH₃ OH 2411 S—(CH₂CH₂)—S PO(OCH₂CH₃)₂ CH₃ OH 2412 S—(CH₂CH₂CH₂)—S PO(OCH₂CH₃)₂ CH₃ OH 2413 —(CH₂)₄— PO(OCH₂CH₃)₂ CH₃ OH 2414 —(CH₂)₅— PO(OCH₂CH₃)₂ CH₃ OH 2415 H H PO(CH₃)₂ CH₃ OH 2416 CH₃ CH₃ PO(CH₃)₂ CH₃ OH 2417 CH₂CH₃ CH₂CH₃ PO(CH₃)₂ CH₃ OH 2418 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₃)₂ CH₃ OH 2419 OCH₃ OCH₃ PO(CH₃)₂ CH₃ OH 2420 OCH₂CH₃ OCH₂CH₃ PO(CH₃)₂ CH₃ OH 2421 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₃)₂ CH₃ OH 2422 SCH₃ SCH₃ PO(CH₃)₂ CH₃ OH 2423 SCH₂CH₃ SCH₂CH₃ PO(CH₃)₂ CH₃ OH 2424 N(CH₃)₂ N(CH₃)₂ PO(CH₃)₂ CH₃ OH 2425 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₃)₂ CH₃ OH 2426 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₃)₂ CH₃ OH 2427 O—(CH₂CH₂)—O PO(CH₃)₂ CH₃ OH 2428 O—(CH₂CH₂CH₂)—O PO(CH₃)₂ CH₃ OH 2429 S—(CH₂CH₂)—S PO(CH₃)₂ CH₃ OH 2430 S—(CH₂CH₂CH₂)—S PO(CH₃)₂ CH₃ OH 2431 —(CH₂)₄— PO(CH₃)₂ CH₃ OH 2432 —(CH₂)₅— PO(CH₃)₂ CH₃ OH 2433 H H PO(CH₂CH₃)₂ CH₃ OH 2434 CH₃ CH₃ PO(CH₂CH₃)₂ CH₃ OH 2435 CH₂CH₃ CH₂CH₃ PO(CH₂CH₃)₂ CH₃ OH 2436 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₂CH₃)₂ CH₃ OH 2437 OCH₃ OCH₃ PO(CH₂CH₃)₂ CH₃ OH 2438 OCH₂CH₃ OCH₂CH₃ PO(CH₂CH₃)₂ CH₃ OH 2439 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₂CH₃)₂ CH₃ OH 2440 SCH₃ SCH₃ PO(CH₂CH₃)₂ CH₃ OH 2441 SCH₂CH₃ SCH₂CH₃ PO(CH₂CH₃)₂ CH₃ OH 2442 N(CH₃)₂ N(CH₃)₂ PO(CH₂CH₃)₂ CH₃ OH 2443 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₂CH₃)₂ CH₃ OH 2444 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₂CH₃)₂ CH₃ OH 2445 O—(CH₂CH₂)—O PO(CH₂CH₃)₂ CH₃ OH 2446 O—(CH₂CH₂CH₂)—O PO(CH₂CH₃)₂ CH₃ OH 2447 S—(CH₂CH₂)—S PO(CH₂CH₃)₂ CH₃ OH 2448 S—(CH₂CH₂CH₂)—S PO(CH₂CH₃)₂ CH₃ OH 2449 —(CH₂)₄— PO(CH₂CH₃)₂ CH₃ OH 2450 —(CH₂)₅— PO(CH₂CH₃)₂ CH₃ OH 2451 H H H CH₃ OCOC₆H₅ 2452 CH₃ CH₃ H CH₃ OCOC₆H₅ 2453 CH₂CH₃ CH₂CH₃ H CH₃ OCOC₆H₅ 2454 CH₂CH₂CH₃ CH₂CH₂CH₃ H CH₃ OCOC₆H₅ 2455 OCH₃ OCH₃ H CH₃ OCOC₆H₅ 2456 OCH₂CH₃ OCH₂CH₃ H CH₃ OCOC₆H₅ 2457 OCH₂CH₂CH₃ OCH₂CH₂CH₃ H CH₃ OCOC₆H₅ 2458 SCH₃ SCH₃ H CH₃ OCOC₆H₅ 2459 SCH₂CH₃ SCH₂CH₃ H CH₃ OCOC₆H₅ 2460 N(CH₃)₂ N(CH₃)₂ H CH₃ OCOC₆H₅ 2461 N(CH₂CH₃)₂ N(CH₂CH₃)₂ H CH₃ OCOC₆H₅ 2462 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) H CH₃ OCOC₆H₅ 2463 O—(CH₂CH₂)—O H CH₃ OCOC₆H₅ 2464 O—(CH₂CH₂CH₂)—O H CH₃ OCOC₆H₅ 2465 S—(CH₂CH₂)—S H CH₃ OCOC₆H₅ 2466 S—(CH₂CH₂CH₂)—S H CH₃ OCOC₆H₅ 2467 —(CH₂)₄— H CH₃ OCOC₆H₅ 2468 —(CH₂)₅— H CH₃ OCOC₆H₅ 2469 H H NO₂ CH₃ OCOC₆H₅ 2470 CH₃ CH₃ NO₂ CH₃ OCOC₆H₅ 2471 CH₂CH₃ CH₂CH₃ NO₂ CH₃ OCOC₆H₅ 2472 CH₂CH₂CH₃ CH₂CH₂CH₃ NO₂ CH₃ OCOC₆H₅ 2473 OCH₃ OCH₃ NO₂ CH₃ OCOC₆H₅ 2474 OCH₂CH₃ OCH₂CH₃ NO₂ CH₃ OCOC₆H₅ 2475 OCH₂CH₂CH₃ OCH₂CH₂CH₃ NO₂ CH₃ OCOC₆H₅ 2476 SCH₃ SCH₃ NO₂ CH₃ OCOC₆H₅ 2477 SCH₂CH₃ SCH₂CH₃ NO₂ CH₃ OCOC₆H₅ 2478 N(CH₃)₂ N(CH₃)₂ NO₂ CH₃ OCOC₆H₅ 2479 N(CH₂CH₃)₂ N(CH₂CH₃)₂ NO₂ CH₃ OCOC₆H₅ 2480 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) NO₂ CH₃ OCOC₆H₅ 2481 O—(CH₂CH₂)—O NO₂ CH₃ OCOC₆H₅ 2482 O—(CH₂CH₂CH₂)—O NO₂ CH₃ OCOC₆H₅ 2483 S—(CH₂CH₂)—S NO₂ CH₃ OCOC₆H₅ 2484 S—(CH₂CH₂CH₂)—S NO₂ CH₃ OCOC₆H₅ 2485 —(CH₂)₄— NO₂ CH₃ OCOC₆H₅ 2486 —(CH₂)₅— NO₂ CH₃ OCOC₆H₅ 2487 H H CN CH₃ OCOC₆H₅ 2488 CH₃ CH₃ CN CH₃ OCOC₆H₅ 2489 CH₂CH₃ CH₂CH₃ CN CH₃ OCOC₆H₅ 2490 CH₂CH₂CH₃ CH₂CH₂CH₃ CN CH₃ OCOC₆H₅ 2491 OCH₃ OCH₃ CN CH₃ OCOC₆H₅ 2492 OCH₂CH₃ OCH₂CH₃ CN CH₃ OCOC₆H₅ 2493 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CN CH₃ OCOC₆H₅ 2494 SCH₃ SCH₃ CN CH₃ OCOC₆H₅ 2495 SCH₂CH₃ SCH₂CH₃ CN CH₃ OCOC₆H₅ 2496 N(CH₃)₂ N(CH₃)₂ CN CH₃ OCOC₆H₅ 2497 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CN CH₃ OCOC₆H₅ 2498 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CN CH₃ OCOC₆H₅ 2499 O—(CH₂CH₂)—O CN CH₃ OCOC₆H₅ 2500 O—(CH₂CH₂CH₂)—O CN CH₃ OCOC₆H₅ 2501 S—(CH₂CH₂)—S CN CH₃ OCOC₆H₅ 2502 S—(CH₂CH₂CH₂)—S CN CH₃ OCOC₆H₅ 2503 —(CH₂)₄— CN CH₃ OCOC₆H₅ 2504 —(CH₂)₅— CN CH₃ OCOC₆H₅ 2505 H H F CH₃ OCOC₆H₅ 2506 CH₃ CH₃ F CH₃ OCOC₆H₅ 2507 CH₂CH₃ CH₂CH₃ F CH₃ OCOC₆H₅ 2508 CH₂CH₂CH₃ CH₂CH₂CH₃ F CH₃ OCOC₆H₅ 2509 OCH₃ OCH₃ F CH₃ OCOC₆H₅ 2510 OCH₂CH₃ OCH₂CH₃ F CH₃ OCOC₆H₅ 2511 OCH₂CH₂CH₃ OCH₂CH₂CH₃ F CH₃ OCOC₆H₅ 2512 SCH₃ SCH₃ F CH₃ OCOC₆H₅ 2513 SCH₂CH₃ SCH₂CH₃ F CH₃ OCOC₆H₅ 2514 N(CH₃)₂ N(CH₃)₂ F CH₃ OCOC₆H₅ 2515 N(CH₂CH₃)₂ N(CH₂CH₃)₂ F CH₃ OCOC₆H₅ 2516 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) F CH₃ OCOC₆H₅ 2517 O—(CH₂CH₂)—O F CH₃ OCOC₆H₅ 2518 O—(CH₂CH₂CH₂)—O F CH₃ OCOC₆H₅ 2519 S—(CH₂CH₂)—S F CH₃ OCOC₆H₅ 2520 S—(CH₂CH₂CH₂)—S F CH₃ OCOC₆H₅ 2521 —(CH₂)₄— F CH₃ OCOC₆H₅ 2522 —(CH₂)₅— F CH₃ OCOC₆H₅ 2523 H H Cl CH₃ OCOC₆H₅ 2524 CH₃ CH₃ Cl CH₃ OCOC₆H₅ 2525 CH₂CH₃ CH₂CH₃ Cl CH₃ OCOC₆H₅ 2526 CH₂CH₂CH₃ CH₂CH₂CH₃ Cl CH₃ OCOC₆H₅ 2527 OCH₃ OCH₃ Cl CH₃ OCOC₆H₅ 2528 OCH₂CH₃ OCH₂CH₃ Cl CH₃ OCOC₆H₅ 2529 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Cl CH₃ OCOC₆H₅ 2530 SCH₃ SCH₃ Cl CH₃ OCOC₆H₅ 2531 SCH₂CH₃ SCH₂CH₃ Cl CH₃ OCOC₆H₅ 2532 N(CH₃)₂ N(CH₃)₂ Cl CH₃ OCOC₆H₅ 2533 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Cl CH₃ OCOC₆H₅ 2534 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Cl CH₃ OCOC₆H₅ 2535 O—(CH₂CH₂)—O Cl CH₃ OCOC₆H₅ 2536 O—(CH₂CH₂CH₂)—O Cl CH₃ OCOC₆H₅ 2537 S—(CH₂CH₂)—S Cl CH₃ OCOC₆H₅ 2538 S—(CH₂CH₂CH₂)—S Cl CH₃ OCOC₆H₅ 2539 —(CH₂)₄— Cl CH₃ OCOC₆H₅ 2540 —(CH₂)₅— Cl CH₃ OCOC₆H₅ 2541 H H Br CH₃ OCOC₆H₅ 2542 CH₃ CH₃ Br CH₃ OCOC₆H₅ 2543 CH₂CH₃ CH₂CH₃ Br CH₃ OCOC₆H₅ 2544 CH₂CH₂CH₃ CH₂CH₂CH₃ Br CH₃ OCOC₆H₅ 2545 OCH₃ OCH₃ Br CH₃ OCOC₆H₅ 2546 OCH₂CH₃ OCH₂CH₃ Br CH₃ OCOC₆H₅ 2547 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Br CH₃ OCOC₆H₅ 2548 SCH₃ SCH₃ Br CH₃ OCOC₆H₅ 2549 SCH₂CH₃ SCH₂CH₃ Br CH₃ OCOC₆H₅ 2550 N(CH₃)₂ N(CH₃)₂ Br CH₃ OCOC₆H₅ 2551 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Br CH₃ OCOC₆H₅ 2552 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Br CH₃ OCOC₆H₅ 2553 O—(CH₂CH₂)—O Br CH₃ OCOC₆H₅ 2554 O—(CH₂CH₂CH₂)—O Br CH₃ OCOC₆H₅ 2555 S—(CH₂CH₂)—S Br CH₃ OCOC₆H₅ 2556 S—(CH₂CH₂CH₂)—S Br CH₃ OCOC₆H₅ 2557 —(CH₂)₄— Br CH₃ OCOC₆H₅ 2558 —(CH₂)₅— Br CH₃ OCOC₆H₅ 2559 H H CH₃ CH₃ OCOC₆H₅ 2560 CH₃ CH₃ CH₃ CH₃ OCOC₆H₅ 2561 CH₂CH₃ CH₂CH₃ CH₃ CH₃ OCOC₆H₅ 2562 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₃ CH₃ OCOC₆H₅ 2563 OCH₃ OCH₃ CH₃ CH₃ OCOC₆H₅ 2564 OCH₂CH₃ OCH₂CH₃ CH₃ CH₃ OCOC₆H₅ 2565 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₃ CH₃ OCOC₆H₅ 2566 SCH₃ SCH₃ CH₃ CH₃ OCOC₆H₅ 2567 SCH₂CH₃ SCH₂CH₃ CH₃ CH₃ OCOC₆H₅ 2568 N(CH₃)₂ N(CH₃)₂ CH₃ CH₃ OCOC₆H₅ 2569 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₃ CH₃ OCOC₆H₅ 2570 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₃ CH₃ OCOC₆H₅ 2571 O—(CH₂CH₂)—O CH₃ CH₃ OCOC₆H₅ 2572 O—(CH₂CH₂CH₂)—O CH₃ CH₃ OCOC₆H₅ 2573 S—(CH₂CH₂)—S CH₃ CH₃ OCOC₆H₅ 2574 S—(CH₂CH₂CH₂)—S CH₃ CH₃ OCOC₆H₅ 2575 —(CH₂)₄— CH₃ CH₃ OCOC₆H₅ 2576 —(CH₂)₅— CH₃ CH₃ OCOC₆H₅ 2577 H H CH₂CH₃ CH₃ OCOC₆H₅ 2578 CH₃ CH₃ CH₂CH₃ CH₃ OCOC₆H₅ 2579 CH₂CH₃ CH₂CH₃ CH₂CH₃ CH₃ OCOC₆H₅ 2580 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₂CH₃ CH₃ OCOC₆H₅ 2581 OCH₃ OCH₃ CH₂CH₃ CH₃ OCOC₆H₅ 2582 OCH₂CH₃ OCH₂CH₃ CH₂CH₃ CH₃ OCOC₆H₅ 2583 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₂CH₃ CH₃ OCOC₆H₅ 2584 SCH₃ SCH₃ CH₂CH₃ CH₃ OCOC₆H₅ 2585 SCH₂CH₃ SCH₂CH₃ CH₂CH₃ CH₃ OCOC₆H₅ 2586 N(CH₃)₂ N(CH₃)₂ CH₂CH₃ CH₃ OCOC₆H₅ 2587 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₂CH₃ CH₃ OCOC₆H₅ 2588 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₂CH₃ CH₃ OCOC₆H₅ 2589 O—(CH₂CH₂)—O CH₂CH₃ CH₃ OCOC₆H₅ 2590 O—(CH₂CH₂CH₂)—O CH₂CH₃ CH₃ OCOC₆H₅ 2591 S—(CH₂CH₂)—S CH₂CH₃ CH₃ OCOC₆H₅ 2592 S—(CH₂CH₂CH₂)—S CH₂CH₃ CH₃ OCOC₆H₅ 2593 —(CH₂)₄— CH₂CH₃ CH₃ OCOC₆H₅ 2594 —(CH₂)₅— CH₂CH₃ CH₃ OCOC₆H₅ 2595 H H CF₃ CH₃ OCOC₆H₅ 2596 CH₃ CH₃ CF₃ CH₃ OCOC₆H₅ 2597 CH₂CH₃ CH₂CH₃ CF₃ CH₃ OCOC₆H₅ 2598 CH₂CH₂CH₃ CH₂CH₂CH₃ CF₃ CH₃ OCOC₆H₅ 2599 OCH₃ OCH₃ CF₃ CH₃ OCOC₆H₅ 2600 OCH₂CH₃ OCH₂CH₃ CF₃ CH₃ OCOC₆H₅ 2601 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CF₃ CH₃ OCOC₆H₅ 2602 SCH₃ SCH₃ CF₃ CH₃ OCOC₆H₅ 2603 SCH₂CH₃ SCH₂CH₃ CF₃ CH₃ OCOC₆H₅ 2604 N(CH₃)₂ N(CH₃)₂ CF₃ CH₃ OCOC₆H₅ 2605 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CF₃ CH₃ OCOC₆H₅ 2606 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CF₃ CH₃ OCOC₆H₅ 2607 O—(CH₂CH₂)—O CF₃ CH₃ OCOC₆H₅ 2608 O—(CH₂CH₂CH₂)—O CF₃ CH₃ OCOC₆H₅ 2609 S—(CH₂CH₂)—S CF₃ CH₃ OCOC₆H₅ 2610 S—(CH₂CH₂CH₂)—S CF₃ CH₃ OCOC₆H₅ 2611 —(CH₂)₄— CF₃ CH₃ OCOC₆H₅ 2612 —(CH₂)₅— CF₃ CH₃ OCOC₆H₅ 2613 H H OCH₃ CH₃ OCOC₆H₅ 2614 CH₃ CH₃ OCH₃ CH₃ OCOC₆H₅ 2615 CH₂CH₃ CH₂CH₃ OCH₃ CH₃ OCOC₆H₅ 2616 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₃ CH₃ OCOC₆H₅ 2617 OCH₃ OCH₃ OCH₃ CH₃ OCOC₆H₅ 2618 OCH₂CH₃ OCH₂CH₃ OCH₃ CH₃ OCOC₆H₅ 2619 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₃ CH₃ OCOC₆H₅ 2620 SCH₃ SCH₃ OCH₃ CH₃ OCOC₆H₅ 2621 SCH₂CH₃ SCH₂CH₃ OCH₃ CH₃ OCOC₆H₅ 2622 N(CH₃)₂ N(CH₃)₂ OCH₃ CH₃ OCOC₆H₅ 2623 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₃ CH₃ OCOC₆H₅ 2624 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₃ CH₃ OCOC₆H₅ 2625 O—(CH₂CH₂)—O OCH₃ CH₃ OCOC₆H₅ 2626 O—(CH₂CH₂CH₂)—O OCH₃ CH₃ OCOC₆H₅ 2627 S—(CH₂CH₂)—S OCH₃ CH₃ OCOC₆H₅ 2628 S—(CH₂CH₂CH₂)—S OCH₃ CH₃ OCOC₆H₅ 2629 —(CH₂)₄— OCH₃ CH₃ OCOC₆H₅ 2630 —(CH₂)₅— OCH₃ CH₃ OCOC₆H₅ 2631 H H OCH₂CH₃ CH₃ OCOC₆H₅ 2632 CH₃ CH₃ OCH₂CH₃ CH₃ OCOC₆H₅ 2633 CH₂CH₃ CH₂CH₃ OCH₂CH₃ CH₃ OCOC₆H₅ 2634 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₂CH₃ CH₃ OCOC₆H₅ 2635 OCH₃ OCH₃ OCH₂CH₃ CH₃ OCOC₆H₅ 2636 OCH₂CH₃ OCH₂CH₃ OCH₂CH₃ CH₃ OCOC₆H₅ 2637 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₂CH₃ CH₃ OCOC₆H₅ 2638 SCH₃ SCH₃ OCH₂CH₃ CH₃ OCOC₆H₅ 2639 SCH₂CH₃ SCH₂CH₃ OCH₂CH₃ CH₃ OCOC₆H₅ 2640 N(CH₃)₂ N(CH₃)₂ OCH₂CH₃ CH₃ OCOC₆H₅ 2641 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₂CH₃ CH₃ OCOC₆H₅ 2642 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₂CH₃ CH₃ OCOC₆H₅ 2643 O—(CH₂CH₂)—O OCH₂CH₃ CH₃ OCOC₆H₅ 2644 O—(CH₂CH₂CH₂)—O OCH₂CH₃ CH₃ OCOC₆H₅ 2645 S—(CH₂CH₂)—S OCH₂CH₃ CH₃ OCOC₆H₅ 2646 S—(CH₂CH₂CH₂)—S OCH₂CH₃ CH₃ OCOC₆H₅ 2647 —(CH₂)₄— OCH₂CH₃ CH₃ OCOC₆H₅ 2648 —(CH₂)₅— OCH₂CH₃ CH₃ OCOC₆H₅ 2649 H H SCH₃ CH₃ OCOC₆H₅ 2650 CH₃ CH₃ SCH₃ CH₃ OCOC₆H₅ 2651 CH₂CH₃ CH₂CH₃ SCH₃ CH₃ OCOC₆H₅ 2652 CH₂CH₂CH₃ CH₂CH₂CH₃ SCH₃ CH₃ OCOC₆H₅ 2653 OCH₃ OCH₃ SCH₃ CH₃ OCOC₆H₅ 2654 OCH₂CH₃ OCH₂CH₃ SCH₃ CH₃ OCOC₆H₅ 2655 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SCH₃ CH₃ OCOC₆H₅ 2656 SCH₃ SCH₃ SCH₃ CH₃ OCOC₆H₅ 2657 SCH₂CH₃ SCH₂CH₃ SCH₃ CH₃ OCOC₆H₅ 2658 N(CH₃)₂ N(CH₃)₂ SCH₃ CH₃ OCOC₆H₅ 2659 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SCH₃ CH₃ OCOC₆H₅ 2660 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SCH₃ CH₃ OCOC₆H₅ 2661 O—(CH₂CH₂)—O SCH₃ CH₃ OCOC₆H₅ 2662 O—(CH₂CH₂CH₂)—O SCH₃ CH₃ OCOC₆H₅ 2663 S—(CH₂CH₂)—S SCH₃ CH₃ OCOC₆H₅ 2664 S—(CH₂CH₂CH₂)—S SCH₃ CH₃ OCOC₆H₅ 2665 —(CH₂)₄— SCH₃ CH₃ OCOC₆H₅ 2666 —(CH₂)₅— SCH₃ CH₃ OCOC₆H₅ 2667 H H SO₂CH₃ CH₃ OCOC₆H₅ 2668 CH₃ CH₃ SO₂CH₃ CH₃ OCOC₆H₅ 2669 CH₂CH₃ CH₂CH₃ SO₂CH₃ CH₃ OCOC₆H₅ 2670 CH₂CH₂CH₃ CH₂CH₂CH₃ SO₂CH₃ CH₃ OCOC₆H₅ 2671 OCH₃ OCH₃ SO₂CH₃ CH₃ OCOC₆H₅ 2672 OCH₂CH₃ OCH₂CH₃ SO₂CH₃ CH₃ OCOC₆H₅ 2673 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SO₂CH₃ CH₃ OCOC₆H₅ 2674 SCH₃ SCH₃ SO₂CH₃ CH₃ OCOC₆H₅ 2675 SCH₂CH₃ SCH₂CH₃ SO₂CH₃ CH₃ OCOC₆H₅ 2676 N(CH₃)₂ N(CH₃)₂ SO₂CH₃ CH₃ OCOC₆H₅ 2677 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SO₂CH₃ CH₃ OCOC₆H₅ 2678 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SO₂CH₃ CH₃ OCOC₆H₅ 2679 O—(CH₂CH₂)—O SO₂CH₃ CH₃ OCOC₆H₅ 2680 O—(CH₂CH₂CH₂)—O SO₂CH₃ CH₃ OCOC₆H₅ 2681 S—(CH₂CH₂)—S SO₂CH₃ CH₃ OCOC₆H₅ 2682 S—(CH₂CH₂CH₂)—S SO₂CH₃ CH₃ OCOC₆H₅ 2683 —(CH₂)₄— SO₂CH₃ CH₃ OCOC₆H₅ 2684 —(CH₂)₅— SO₂CH₃ CH₃ OCOC₆H₅ 2685 H H PO(OCH₃)₂ CH₃ OCOC₆H₅ 2686 CH₃ CH₃ PO(OCH₃)₂ CH₃ OCOC₆H₅ 2687 CH₂CH₃ CH₂CH₃ PO(OCH₃)₂ CH₃ OCOC₆H₅ 2688 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₃)₂ CH₃ OCOC₆H₅ 2689 OCH₃ OCH₃ PO(OCH₃)₂ CH₃ OCOC₆H₅ 2690 OCH₂CH₃ OCH₂CH₃ PO(OCH₃)₂ CH₃ OCOC₆H₅ 2691 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₃)₂ CH₃ OCOC₆H₅ 2692 SCH₃ SCH₃ PO(OCH₃)₂ CH₃ OCOC₆H₅ 2693 SCH₂CH₃ SCH₂CH₃ PO(OCH₃)₂ CH₃ OCOC₆H₅ 2694 N(CH₃)₂ N(CH₃)₂ PO(OCH₃)₂ CH₃ OCOC₆H₅ 2695 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₃)₂ CH₃ OCOC₆H₅ 2696 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₃)₂ CH₃ OCOC₆H₅ 2697 O—(CH₂CH₂)—O PO(OCH₃)₂ CH₃ OCOC₆H₅ 2698 O—(CH₂CH₂CH₂)—O PO(OCH₃)₂ CH₃ OCOC₆H₅ 2699 S—(CH₂CH₂)—S PO(OCH₃)₂ CH₃ OCOC₆H₅ 2700 S—(CH₂CH₂CH₂)—S PO(OCH₃)₂ CH₃ OCOC₆H₅ 2701 —(CH₂)₄— PO(OCH₃)₂ CH₃ OCOC₆H₅ 2702 —(CH₂)₅— PO(OCH₃)₂ CH₃ OCOC₆H₅ 2703 H H PO(OCH₂CH₃)₂ CH₃ OCOC₆H₅ 2704 CH₃ CH₃ PO(OCH₂CH₃)₂ CH₃ OCOC₆H₅ 2705 CH₂CH₃ CH₂CH₃ PO(OCH₂CH₃)₂ CH₃ OCOC₆H₅ 2706 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₂CH₃)₂ CH₃ OCOC₆H₅ 2707 OCH₃ OCH₃ PO(OCH₂CH₃)₂ CH₃ OCOC₆H₅ 2708 OCH₂CH₃ OCH₂CH₃ PO(OCH₂CH₃)₂ CH₃ OCOC₆H₅ 2709 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₂CH₃)₂ CH₃ OCOC₆H₅ 2710 SCH₃ SCH₃ PO(OCH₂CH₃)₂ CH₃ OCOC₆H₅ 2711 SCH₂CH₃ SCH₂CH₃ PO(OCH₂CH₃)₂ CH₃ OCOC₆H₅ 2712 N(CH₃)₂ N(CH₃)₂ PO(OCH₂CH₃)₂ CH₃ OCOC₆H₅ 2713 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₂CH₃)₂ CH₃ OCOC₆H₅ 2714 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₂CH₃)₂ CH₃ OCOC₆H₅ 2715 O—(CH₂CH₂)—O PO(OCH₂CH₃)₂ CH₃ OCOC₆H₅ 2716 O—(CH₂CH₂CH₂)—O PO(OCH₂CH₃)₂ CH₃ OCOC₆H₅ 2717 S—(CH₂CH₂)—S PO(OCH₂CH₃)₂ CH₃ OCOC₆H₅ 2718 S—(CH₂CH₂CH₂)—S PO(OCH₂CH₃)₂ CH₃ OCOC₆H₅ 2719 —(CH₂)₄— PO(OCH₂CH₃)₂ CH₃ OCOC₆H₅ 2720 —(CH₂)₅— PO(OCH₂CH₃)₂ CH₃ OCOC₆H₅ 2721 H H PO(CH₃)₂ CH₃ OCOC₆H₅ 2722 CH₃ CH₃ PO(CH₃)₂ CH₃ OCOC₆H₅ 2723 CH₂CH₃ CH₂CH₃ PO(CH₃)₂ CH₃ OCOC₆H₅ 2724 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₃)₂ CH₃ OCOC₆H₅ 2725 OCH₃ OCH₃ PO(CH₃)₂ CH₃ OCOC₆H₅ 2726 OCH₂CH₃ OCH₂CH₃ PO(CH₃)₂ CH₃ OCOC₆H₅ 2727 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₃)₂ CH₃ OCOC₆H₅ 2728 SCH₃ SCH₃ PO(CH₃)₂ CH₃ OCOC₆H₅ 2729 SCH₂CH₃ SCH₂CH₃ PO(CH₃)₂ CH₃ OCOC₆H₅ 2730 N(CH₃)₂ N(CH₃)₂ PO(CH₃)₂ CH₃ OCOC₆H₅ 2731 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₃)₂ CH₃ OCOC₆H₅ 2732 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₃)₂ CH₃ OCOC₆H₅ 2733 O—(CH₂CH₂)—O PO(CH₃)₂ CH₃ OCOC₆H₅ 2734 O—(CH₂CH₂CH₂)—O PO(CH₃)₂ CH₃ OCOC₆H₅ 2735 S—(CH₂CH₂)—S PO(CH₃)₂ CH₃ OCOC₆H₅ 2736 S—(CH₂CH₂CH₂)—S PO(CH₃)₂ CH₃ OCOC₆H₅ 2737 —(CH₂)₄— PO(CH₃)₂ CH₃ OCOC₆H₅ 2738 —(CH₂)₅— PO(CH₃)₂ CH₃ OCOC₆H₅ 2739 H H PO(CH₂CH₃)₂ CH₃ OCOC₆H₅ 2740 CH₃ CH₃ PO(CH₂CH₃)₂ CH₃ OCOC₆H₅ 2741 CH₂CH₃ CH₂CH₃ PO(CH₂CH₃)₂ CH₃ OCOC₆H₅ 2742 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₂CH₃)₂ CH₃ OCOC₆H₅ 2743 OCH₃ OCH₃ PO(CH₂CH₃)₂ CH₃ OCOC₆H₅ 2744 OCH₂CH₃ OCH₂CH₃ PO(CH₂CH₃)₂ CH₃ OCOC₆H₅ 2745 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₂CH₃)₂ CH₃ OCOC₆H₅ 2746 SCH₃ SCH₃ PO(CH₂CH₃)₂ CH₃ OCOC₆H₅ 2747 SCH₂CH₃ SCH₂CH₃ PO(CH₂CH₃)₂ CH₃ OCOC₆H₅ 2748 N(CH₃)₂ N(CH₃)₂ PO(CH₂CH₃)₂ CH₃ OCOC₆H₅ 2749 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₂CH₃)₂ CH₃ OCOC₆H₅ 2750 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₂CH₃)₂ CH₃ OCOC₆H₅ 2751 O—(CH₂CH₂)—O PO(CH₂CH₃)₂ CH₃ OCOC₆H₅ 2752 O—(CH₂CH₂CH₂)—O PO(CH₂CH₃)₂ CH₃ OCOC₆H₅ 2753 S—(CH₂CH₂)—S PO(CH₂CH₃)₂ CH₃ OCOC₆H₅ 2754 S—(CH₂CH₂CH₂)—S PO(CH₂CH₃)₂ CH₃ OCOC₆H₅ 2755 —(CH₂)₄— PO(CH₂CH₃)₂ CH₃ OCOC₆H₅ 2756 —(CH₂)₅— PO(CH₂CH₃)₂ CH₃ OCOC₆H₅ 2757 H H H CH₃ SCH₃ 2758 CH₃ CH₃ H CH₃ SCH₃ 2759 CH₂CH₃ CH₂CH₃ H CH₃ SCH₃ 2760 CH₂CH₂CH₃ CH₂CH₂CH₃ H CH₃ SCH₃ 2761 OCH₃ OCH₃ H CH₃ SCH₃ 2762 OCH₂CH₃ OCH₂CH₃ H CH₃ SCH₃ 2763 OCH₂CH₂CH₃ OCH₂CH₂CH₃ H CH₃ SCH₃ 2764 SCH₃ SCH₃ H CH₃ SCH₃ 2765 SCH₂CH₃ SCH₂CH₃ H CH₃ SCH₃ 2766 N(CH₃)₂ N(CH₃)₂ H CH₃ SCH₃ 2767 N(CH₂CH₃)₂ N(CH₂CH₃)₂ H CH₃ SCH₃ 2768 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) H CH₃ SCH₃ 2769 O—(CH₂CH₂)—O H CH₃ SCH₃ 2770 O—(CH₂CH₂CH₂)—O H CH₃ SCH₃ 2771 S—(CH₂CH₂)—S H CH₃ SCH₃ 2772 S—(CH₂CH₂CH₂)—S H CH₃ SCH₃ 2773 —(CH₂)₄— H CH₃ SCH₃ 2774 —(CH₂)₅— H CH₃ SCH₃ 2775 H H NO₂ CH₃ SCH₃ 2776 CH₃ CH₃ NO₂ CH₃ SCH₃ 2777 CH₂CH₃ CH₂CH₃ NO₂ CH₃ SCH₃ 2778 CH₂CH₂CH₃ CH₂CH₂CH₃ NO₂ CH₃ SCH₃ 2779 OCH₃ OCH₃ NO₂ CH₃ SCH₃ 2780 OCH₂CH₃ OCH₂CH₃ NO₂ CH₃ SCH₃ 2781 OCH₂CH₂CH₃ OCH₂CH₂CH₃ NO₂ CH₃ SCH₃ 2782 SCH₃ SCH₃ NO₂ CH₃ SCH₃ 2783 SCH₂CH₃ SCH₂CH₃ NO₂ CH₃ SCH₃ 2784 N(CH₃)₂ N(CH₃)₂ NO₂ CH₃ SCH₃ 2785 N(CH₂CH₃)₂ N(CH₂CH₃)₂ NO₂ CH₃ SCH₃ 2786 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) NO₂ CH₃ SCH₃ 2787 O—(CH₂CH₂)—O NO₂ CH₃ SCH₃ 2788 O—(CH₂CH₂CH₂)—O NO₂ CH₃ SCH₃ 2789 S—(CH₂CH₂)—S NO₂ CH₃ SCH₃ 2790 S—(CH₂CH₂CH₂)—S NO₂ CH₃ SCH₃ 2791 —(CH₂)₄— NO₂ CH₃ SCH₃ 2792 —(CH₂)₅— NO₂ CH₃ SCH₃ 2793 H H CN CH₃ SCH₃ 2794 CH₃ CH₃ CN CH₃ SCH₃ 2795 CH₂CH₃ CH₂CH₃ CN CH₃ SCH₃ 2796 CH₂CH₂CH₃ CH₂CH₂CH₃ CN CH₃ SCH₃ 2797 OCH₃ OCH₃ CN CH₃ SCH₃ 2798 OCH₂CH₃ OCH₂CH₃ CN CH₃ SCH₃ 2799 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CN CH₃ SCH₃ 2800 SCH₃ SCH₃ CN CH₃ SCH₃ 2801 SCH₂CH₃ SCH₂CH₃ CN CH₃ SCH₃ 2802 N(CH₃)₂ N(CH₃)₂ CN CH₃ SCH₃ 2803 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CN CH₃ SCH₃ 2804 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CN CH₃ SCH₃ 2805 O—(CH₂CH₂)—O CN CH₃ SCH₃ 2806 O—(CH₂CH₂CH₂)—O CN CH₃ SCH₃ 2807 S—(CH₂CH₂)—S CN CH₃ SCH₃ 2808 S—(CH₂CH₂CH₂)—S CN CH₃ SCH₃ 2809 —(CH₂)₄— CN CH₃ SCH₃ 2810 —(CH₂)₅— CN CH₃ SCH₃ 2811 H H F CH₃ SCH₃ 2812 CH₃ CH₃ F CH₃ SCH₃ 2813 CH₂CH₃ CH₂CH₃ F CH₃ SCH₃ 2814 CH₂CH₂CH₃ CH₂CH₂CH₃ F CH₃ SCH₃ 2815 OCH₃ OCH₃ F CH₃ SCH₃ 2816 OCH₂CH₃ OCH₂CH₃ F CH₃ SCH₃ 2817 OCH₂CH₂CH₃ OCH₂CH₂CH₃ F CH₃ SCH₃ 2818 SCH₃ SCH₃ F CH₃ SCH₃ 2819 SCH₂CH₃ SCH₂CH₃ F CH₃ SCH₃ 2820 N(CH₃)₂ N(CH₃)₂ F CH₃ SCH₃ 2821 N(CH₂CH₃)₂ N(CH₂CH₃)₂ F CH₃ SCH₃ 2822 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) F CH₃ SCH₃ 2823 O—(CH₂CH₂)—O F CH₃ SCH₃ 2824 O—(CH₂CH₂CH₂)—O F CH₃ SCH₃ 2825 S—(CH₂CH₂)—S F CH₃ SCH₃ 2826 S—(CH₂CH₂CH₂)—S F CH₃ SCH₃ 2827 —(CH₂)₄— F CH₃ SCH₃ 2828 —(CH₂)₅— F CH₃ SCH₃ 2829 H H Cl CH₃ SCH₃ 2830 CH₃ CH₃ Cl CH₃ SCH₃ 2831 CH₂CH₃ CH₂CH₃ Cl CH₃ SCH₃ 2832 CH₂CH₂CH₃ CH₂CH₂CH₃ Cl CH₃ SCH₃ 2833 OCH₃ OCH₃ Cl CH₃ SCH₃ 2834 OCH₂CH₃ OCH₂CH₃ Cl CH₃ SCH₃ 2835 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Cl CH₃ SCH₃ 2836 SCH₃ SCH₃ Cl CH₃ SCH₃ 2837 SCH₂CH₃ SCH₂CH₃ Cl CH₃ SCH₃ 2838 N(CH₃)₂ N(CH₃)₂ Cl CH₃ SCH₃ 2839 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Cl CH₃ SCH₃ 2840 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Cl CH₃ SCH₃ 2841 O—(CH₂CH₂)—O Cl CH₃ SCH₃ 2842 O—(CH₂CH₂CH₂)—O Cl CH₃ SCH₃ 2843 S—(CH₂CH₂)—S Cl CH₃ SCH₃ 2844 S—(CH₂CH₂CH₂)—S Cl CH₃ SCH₃ 2845 —(CH₂)₄— Cl CH₃ SCH₃ 2846 —(CH₂)₅— Cl CH₃ SCH₃ 2847 H H Br CH₃ SCH₃ 2848 CH₃ CH₃ Br CH₃ SCH₃ 2849 CH₂CH₃ CH₂CH₃ Br CH₃ SCH₃ 2850 CH₂CH₂CH₃ CH₂CH₂CH₃ Br CH₃ SCH₃ 2851 OCH₃ OCH₃ Br CH₃ SCH₃ 2852 OCH₂CH₃ OCH₂CH₃ Br CH₃ SCH₃ 2853 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Br CH₃ SCH₃ 2854 SCH₃ SCH₃ Br CH₃ SCH₃ 2855 SCH₂CH₃ SCH₂CH₃ Br CH₃ SCH₃ 2856 N(CH₃)₂ N(CH₃)₂ Br CH₃ SCH₃ 2857 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Br CH₃ SCH₃ 2858 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Br CH₃ SCH₃ 2859 O—(CH₂CH₂)—O Br CH₃ SCH₃ 2860 O—(CH₂CH₂CH₂)—O Br CH₃ SCH₃ 2861 S—(CH₂CH₂)—S Br CH₃ SCH₃ 2862 S—(CH₂CH₂CH₂)—S Br CH₃ SCH₃ 2863 —(CH₂)₄— Br CH₃ SCH₃ 2864 —(CH₂)₅— Br CH₃ SCH₃ 2865 H H CH₃ CH₃ SCH₃ 2866 CH₃ CH₃ CH₃ CH₃ SCH₃ 2867 CH₂CH₃ CH₂CH₃ CH₃ CH₃ SCH₃ 2868 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₃ CH₃ SCH₃ 2869 OCH₃ OCH₃ CH₃ CH₃ SCH₃ 2870 OCH₂CH₃ OCH₂CH₃ CH₃ CH₃ SCH₃ 2871 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₃ CH₃ SCH₃ 2872 SCH₃ SCH₃ CH₃ CH₃ SCH₃ 2873 SCH₂CH₃ SCH₂CH₃ CH₃ CH₃ SCH₃ 2874 N(CH₃)₂ N(CH₃)₂ CH₃ CH₃ SCH₃ 2875 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₃ CH₃ SCH₃ 2876 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₃ CH₃ SCH₃ 2877 O—(CH₂CH₂)—O CH₃ CH₃ SCH₃ 2878 O—(CH₂CH₂CH₂)—O CH₃ CH₃ SCH₃ 2879 S—(CH₂CH₂)—S CH₃ CH₃ SCH₃ 2880 S—(CH₂CH₂CH₂)—S CH₃ CH₃ SCH₃ 2881 —(CH₂)₄— CH₃ CH₃ SCH₃ 2882 —(CH₂)₅— CH₃ CH₃ SCH₃ 2883 H H CH₂CH₃ CH₃ SCH₃ 2884 CH₃ CH₃ CH₂CH₃ CH₃ SCH₃ 2885 CH₂CH₃ CH₂CH₃ CH₂CH₃ CH₃ SCH₃ 2886 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₂CH₃ CH₃ SCH₃ 2887 OCH₃ OCH₃ CH₂CH₃ CH₃ SCH₃ 2888 OCH₂CH₃ OCH₂CH₃ CH₂CH₃ CH₃ SCH₃ 2889 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₂CH₃ CH₃ SCH₃ 2890 SCH₃ SCH₃ CH₂CH₃ CH₃ SCH₃ 2891 SCH₂CH₃ SCH₂CH₃ CH₂CH₃ CH₃ SCH₃ 2892 N(CH₃)₂ N(CH₃)₂ CH₂CH₃ CH₃ SCH₃ 2893 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₂CH₃ CH₃ SCH₃ 2894 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₂CH₃ CH₃ SCH₃ 2895 O—(CH₂CH₂)—O CH₂CH₃ CH₃ SCH₃ 2896 O—(CH₂CH₂CH₂)—O CH₂CH₃ CH₃ SCH₃ 2897 S—(CH₂CH₂)—S CH₂CH₃ CH₃ SCH₃ 2898 S—(CH₂CH₂CH₂)—S CH₂CH₃ CH₃ SCH₃ 2899 —(CH₂)₄— CH₂CH₃ CH₃ SCH₃ 2900 —(CH₂)₅— CH₂CH₃ CH₃ SCH₃ 2901 H H CF₃ CH₃ SCH₃ 2902 CH₃ CH₃ CF₃ CH₃ SCH₃ 2903 CH₂CH₃ CH₂CH₃ CF₃ CH₃ SCH₃ 2904 CH₂CH₂CH₃ CH₂CH₂CH₃ CF₃ CH₃ SCH₃ 2905 OCH₃ OCH₃ CF₃ CH₃ SCH₃ 2906 OCH₂CH₃ OCH₂CH₃ CF₃ CH₃ SCH₃ 2907 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CF₃ CH₃ SCH₃ 2908 SCH₃ SCH₃ CF₃ CH₃ SCH₃ 2909 SCH₂CH₃ SCH₂CH₃ CF₃ CH₃ SCH₃ 2910 N(CH₃)₂ N(CH₃)₂ CF₃ CH₃ SCH₃ 2911 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CF₃ CH₃ SCH₃ 2912 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CF₃ CH₃ SCH₃ 2913 O—(CH₂CH₂)—O CF₃ CH₃ SCH₃ 2914 O—(CH₂CH₂CH₂)—O CF₃ CH₃ SCH₃ 2915 S—(CH₂CH₂)—S CF₃ CH₃ SCH₃ 2916 S—(CH₂CH₂CH₂)—S CF₃ CH₃ SCH₃ 2917 —(CH₂)₄— CF₃ CH₃ SCH₃ 2918 —(CH₂)₅— CF₃ CH₃ SCH₃ 2919 H H OCH₃ CH₃ SCH₃ 2920 CH₃ CH₃ OCH₃ CH₃ SCH₃ 2921 CH₂CH₃ CH₂CH₃ OCH₃ CH₃ SCH₃ 2922 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₃ CH₃ SCH₃ 2923 OCH₃ OCH₃ OCH₃ CH₃ SCH₃ 2924 OCH₂CH₃ OCH₂CH₃ OCH₃ CH₃ SCH₃ 2925 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₃ CH₃ SCH₃ 2926 SCH₃ SCH₃ OCH₃ CH₃ SCH₃ 2927 SCH₂CH₃ SCH₂CH₃ OCH₃ CH₃ SCH₃ 2928 N(CH₃)₂ N(CH₃)₂ OCH₃ CH₃ SCH₃ 2929 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₃ CH₃ SCH₃ 2930 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₃ CH₃ SCH₃ 2931 O—(CH₂CH₂)—O OCH₃ CH₃ SCH₃ 2932 O—(CH₂CH₂CH₂)—O OCH₃ CH₃ SCH₃ 2933 S—(CH₂CH₂)—S OCH₃ CH₃ SCH₃ 2934 S—(CH₂CH₂CH₂)—S OCH₃ CH₃ SCH₃ 2935 —(CH₂)₄— OCH₃ CH₃ SCH₃ 2936 —(CH₂)₅— OCH₃ CH₃ SCH₃ 2937 H H OCH₂CH₃ CH₃ SCH₃ 2938 CH₃ CH₃ OCH₂CH₃ CH₃ SCH₃ 2939 CH₂CH₃ CH₂CH₃ OCH₂CH₃ CH₃ SCH₃ 2940 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₂CH₃ CH₃ SCH₃ 2941 OCH₃ OCH₃ OCH₂CH₃ CH₃ SCH₃ 2942 OCH₂CH₃ OCH₂CH₃ OCH₂CH₃ CH₃ SCH₃ 2943 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₂CH₃ CH₃ SCH₃ 2944 SCH₃ SCH₃ OCH₂CH₃ CH₃ SCH₃ 2945 SCH₂CH₃ SCH₂CH₃ OCH₂CH₃ CH₃ SCH₃ 2946 N(CH₃)₂ N(CH₃)₂ OCH₂CH₃ CH₃ SCH₃ 2947 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₂CH₃ CH₃ SCH₃ 2948 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₂CH₃ CH₃ SCH₃ 2949 O—(CH₂CH₂)—O OCH₂CH₃ CH₃ SCH₃ 2950 O—(CH₂CH₂CH₂)—O OCH₂CH₃ CH₃ SCH₃ 2951 S—(CH₂CH₂)—S OCH₂CH₃ CH₃ SCH₃ 2952 S—(CH₂CH₂CH₂)—S OCH₂CH₃ CH₃ SCH₃ 2953 —(CH₂)₄— OCH₂CH₃ CH₃ SCH₃ 2954 —(CH₂)₅— OCH₂CH₃ CH₃ SCH₃ 2955 H H SCH₃ CH₃ SCH₃ 2956 CH₃ CH₃ SCH₃ CH₃ SCH₃ 2957 CH₂CH₃ CH₂CH₃ SCH₃ CH₃ SCH₃ 2958 CH₂CH₂CH₃ CH₂CH₂CH₃ SCH₃ CH₃ SCH₃ 2959 OCH₃ OCH₃ SCH₃ CH₃ SCH₃ 2960 OCH₂CH₃ OCH₂CH₃ SCH₃ CH₃ SCH₃ 2961 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SCH₃ CH₃ SCH₃ 2962 SCH₃ SCH₃ SCH₃ CH₃ SCH₃ 2963 SCH₂CH₃ SCH₂CH₃ SCH₃ CH₃ SCH₃ 2964 N(CH₃)₂ N(CH₃)₂ SCH₃ CH₃ SCH₃ 2965 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SCH₃ CH₃ SCH₃ 2966 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SCH₃ CH₃ SCH₃ 2967 O—(CH₂CH₂)—O SCH₃ CH₃ SCH₃ 2968 O—(CH₂CH₂CH₂)—O SCH₃ CH₃ SCH₃ 2969 S—(CH₂CH₂)—S SCH₃ CH₃ SCH₃ 2970 S—(CH₂CH₂CH₂)—S SCH₃ CH₃ SCH₃ 2971 —(CH₂)₄— SCH₃ CH₃ SCH₃ 2972 —(CH₂)₅— SCH₃ CH₃ SCH₃ 2973 H H SO₂CH₃ CH₃ SCH₃ 2974 CH₃ CH₃ SO₂CH₃ CH₃ SCH₃ 2975 CH₂CH₃ CH₂CH₃ SO₂CH₃ CH₃ SCH₃ 2976 CH₂CH₂CH₃ CH₂CH₂CH₃ SO₂CH₃ CH₃ SCH₃ 2977 OCH₃ OCH₃ SO₂CH₃ CH₃ SCH₃ 2978 OCH₂CH₃ OCH₂CH₃ SO₂CH₃ CH₃ SCH₃ 2979 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SO₂CH₃ CH₃ SCH₃ 2980 SCH₃ SCH₃ SO₂CH₃ CH₃ SCH₃ 2981 SCH₂CH₃ SCH₂CH₃ SO₂CH₃ CH₃ SCH₃ 2982 N(CH₃)₂ N(CH₃)₂ SO₂CH₃ CH₃ SCH₃ 2983 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SO₂CH₃ CH₃ SCH₃ 2984 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SO₂CH₃ CH₃ SCH₃ 2985 O—(CH₂CH₂)—O SO₂CH₃ CH₃ SCH₃ 2986 O—(CH₂CH₂CH₂)—O SO₂CH₃ CH₃ SCH₃ 2987 S—(CH₂CH₂)—S SO₂CH₃ CH₃ SCH₃ 2988 S—(CH₂CH₂CH₂)—S SO₂CH₃ CH₃ SCH₃ 2989 —(CH₂)₄— SO₂CH₃ CH₃ SCH₃ 2990 —(CH₂)₅— SO₂CH₃ CH₃ SCH₃ 2991 H H PO(OCH₃)₂ CH₃ SCH₃ 2992 CH₃ CH₃ PO(OCH₃)₂ CH₃ SCH₃ 2993 CH₂CH₃ CH₂CH₃ PO(OCH₃)₂ CH₃ SCH₃ 2994 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₃)₂ CH₃ SCH₃ 2995 OCH₃ OCH₃ PO(OCH₃)₂ CH₃ SCH₃ 2996 OCH₂CH₃ OCH₂CH₃ PO(OCH₃)₂ CH₃ SCH₃ 2997 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₃)₂ CH₃ SCH₃ 2998 SCH₃ SCH₃ PO(OCH₃)₂ CH₃ SCH₃ 2999 SCH₂CH₃ SCH₂CH₃ PO(OCH₃)₂ CH₃ SCH₃ 3000 N(CH₃)₂ N(CH₃)₂ PO(OCH₃)₂ CH₃ SCH₃ 3001 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₃)₂ CH₃ SCH₃ 3002 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₃)₂ CH₃ SCH₃ 3003 O—(CH₂CH₂)—O PO(OCH₃)₂ CH₃ SCH₃ 3004 O—(CH₂CH₂CH₂)—O PO(OCH₃)₂ CH₃ SCH₃ 3005 S—(CH₂CH₂)—S PO(OCH₃)₂ CH₃ SCH₃ 3006 S—(CH₂CH₂CH₂)—S PO(OCH₃)₂ CH₃ SCH₃ 3007 —(CH₂)₄— PO(OCH₃)₂ CH₃ SCH₃ 3008 —(CH₂)₅— PO(OCH₃)₂ CH₃ SCH₃ 3009 H H PO(OCH₂CH₃)₂ CH₃ SCH₃ 3010 CH₃ CH₃ PO(OCH₂CH₃)₂ CH₃ SCH₃ 3011 CH₂CH₃ CH₂CH₃ PO(OCH₂CH₃)₂ CH₃ SCH₃ 3012 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₂CH₃)₂ CH₃ SCH₃ 3013 OCH₃ OCH₃ PO(OCH₂CH₃)₂ CH₃ SCH₃ 3014 OCH₂CH₃ OCH₂CH₃ PO(OCH₂CH₃)₂ CH₃ SCH₃ 3015 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₂CH₃)₂ CH₃ SCH₃ 3016 SCH₃ SCH₃ PO(OCH₂CH₃)₂ CH₃ SCH₃ 3017 SCH₂CH₃ SCH₂CH₃ PO(OCH₂CH₃)₂ CH₃ SCH₃ 3018 N(CH₃)₂ N(CH₃)₂ PO(OCH₂CH₃)₂ CH₃ SCH₃ 3019 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₂CH₃)₂ CH₃ SCH₃ 3020 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₂CH₃)₂ CH₃ SCH₃ 3021 O—(CH₂CH₂)—O PO(OCH₂CH₃)₂ CH₃ SCH₃ 3022 O—(CH₂CH₂CH₂)—O PO(OCH₂CH₃)₂ CH₃ SCH₃ 3023 S—(CH₂CH₂)—S PO(OCH₂CH₃)₂ CH₃ SCH₃ 3024 S—(CH₂CH₂CH₂)—S PO(OCH₂CH₃)₂ CH₃ SCH₃ 3025 —(CH₂)₄— PO(OCH₂CH₃)₂ CH₃ SCH₃ 3026 —(CH₂)₅— PO(OCH₂CH₃)₂ CH₃ SCH₃ 3027 H H PO(CH₃)₂ CH₃ SCH₃ 3028 CH₃ CH₃ PO(CH₃)₂ CH₃ SCH₃ 3029 CH₂CH₃ CH₂CH₃ PO(CH₃)₂ CH₃ SCH₃ 3030 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₃)₂ CH₃ SCH₃ 3031 OCH₃ OCH₃ PO(CH₃)₂ CH₃ SCH₃ 3032 OCH₂CH₃ OCH₂CH₃ PO(CH₃)₂ CH₃ SCH₃ 3033 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₃)₂ CH₃ SCH₃ 3034 SCH₃ SCH₃ PO(CH₃)₂ CH₃ SCH₃ 3035 SCH₂CH₃ SCH₂CH₃ PO(CH₃)₂ CH₃ SCH₃ 3036 N(CH₃)₂ N(CH₃)₂ PO(CH₃)₂ CH₃ SCH₃ 3037 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₃)₂ CH₃ SCH₃ 3038 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₃)₂ CH₃ SCH₃ 3039 O—(CH₂CH₂)—O PO(CH₃)₂ CH₃ SCH₃ 3040 O—(CH₂CH₂CH₂)—O PO(CH₃)₂ CH₃ SCH₃ 3041 S—(CH₂CH₂)—S PO(CH₃)₂ CH₃ SCH₃ 3042 S—(CH₂CH₂CH₂)—S PO(CH₃)₂ CH₃ SCH₃ 3043 —(CH₂)₄— PO(CH₃)₂ CH₃ SCH₃ 3044 —(CH₂)₅— PO(CH₃)₂ CH₃ SCH₃ 3045 H H PO(CH₂CH₃)₂ CH₃ SCH₃ 3046 CH₃ CH₃ PO(CH₂CH₃)₂ CH₃ SCH₃ 3047 CH₂CH₃ CH₂CH₃ PO(CH₂CH₃)₂ CH₃ SCH₃ 3048 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₂CH₃)₂ CH₃ SCH₃ 3049 OCH₃ OCH₃ PO(CH₂CH₃)₂ CH₃ SCH₃ 3050 OCH₂CH₃ OCH₂CH₃ PO(CH₂CH₃)₂ CH₃ SCH₃ 3051 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₂CH₃)₂ CH₃ SCH₃ 3052 SCH₃ SCH₃ PO(CH₂CH₃)₂ CH₃ SCH₃ 3053 SCH₂CH₃ SCH₂CH₃ PO(CH₂CH₃)₂ CH₃ SCH₃ 3054 N(CH₃)₂ N(CH₃)₂ PO(CH₂CH₃)₂ CH₃ SCH₃ 3055 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₂CH₃)₂ CH₃ SCH₃ 3056 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₂CH₃)₂ CH₃ SCH₃ 3057 O—(CH₂CH₂)—O PO(CH₂CH₃)₂ CH₃ SCH₃ 3058 O—(CH₂CH₂CH₂)—O PO(CH₂CH₃)₂ CH₃ SCH₃ 3059 S—(CH₂CH₂)—S PO(CH₂CH₃)₂ CH₃ SCH₃ 3060 S—(CH₂CH₂CH₂)—S PO(CH₂CH₃)₂ CH₃ SCH₃ 3061 —(CH₂)₄— PO(CH₂CH₃)₂ CH₃ SCH₃ 3062 —(CH₂)₅— PO(CH₂CH₃)₂ CH₃ SCH₃ 3063 H H H CH₃ SC₆H₅ 3064 CH₃ CH₃ H CH₃ SC₆H₅ 3065 CH₂CH₃ CH₂CH₃ H CH₃ SC₆H₅ 3066 CH₂CH₂CH₃ CH₂CH₂CH₃ H CH₃ SC₆H₅ 3067 OCH₃ OCH₃ H CH₃ SC₆H₅ 3068 OCH₂CH₃ OCH₂CH₃ H CH₃ SC₆H₅ 3069 OCH₂CH₂CH₃ OCH₂CH₂CH₃ H CH₃ SC₆H₅ 3070 SCH₃ SCH₃ H CH₃ SC₆H₅ 3071 SCH₂CH₃ SCH₂CH₃ H CH₃ SC₆H₅ 3072 N(CH₃)₂ N(CH₃)₂ H CH₃ SC₆H₅ 3073 N(CH₂CH₃)₂ N(CH₂CH₃)₂ H CH₃ SC₆H₅ 3074 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) H CH₃ SC₆H₅ 3075 O—(CH₂CH₂)—O H CH₃ SC₆H₅ 3076 O—(CH₂CH₂CH₂)—O H CH₃ SC₆H₅ 3077 S—(CH₂CH₂)—S H CH₃ SC₆H₅ 3078 S—(CH₂CH₂CH₂)—S H CH₃ SC₆H₅ 3079 —(CH₂)₄— H CH₃ SC₆H₅ 3080 —(CH₂)₅— H CH₃ SC₆H₅ 3081 H H NO₂ CH₃ SC₆H₅ 3082 CH₃ CH₃ NO₂ CH₃ SC₆H₅ 3083 CH₂CH₃ CH₂CH₃ NO₂ CH₃ SC₆H₅ 3084 CH₂CH₂CH₃ CH₂CH₂CH₃ NO₂ CH₃ SC₆H₅ 3085 OCH₃ OCH₃ NO₂ CH₃ SC₆H₅ 3086 OCH₂CH₃ OCH₂CH₃ NO₂ CH₃ SC₆H₅ 3087 OCH₂CH₂CH₃ OCH₂CH₂CH₃ NO₂ CH₃ SC₆H₅ 3088 SCH₃ SCH₃ NO₂ CH₃ SC₆H₅ 3089 SCH₂CH₃ SCH₂CH₃ NO₂ CH₃ SC₆H₅ 3090 N(CH₃)₂ N(CH₃)₂ NO₂ CH₃ SC₆H₅ 3091 N(CH₂CH₃)₂ N(CH₂CH₃)₂ NO₂ CH₃ SC₆H₅ 3092 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) NO₂ CH₃ SC₆H₅ 3093 O—(CH₂CH₂)—O NO₂ CH₃ SC₆H₅ 3094 O—(CH₂CH₂CH₂)—O NO₂ CH₃ SC₆H₅ 3095 S—(CH₂CH₂)—S NO₂ CH₃ SC₆H₅ 3096 S—(CH₂CH₂CH₂)—S NO₂ CH₃ SC₆H₅ 3097 —(CH₂)₄— NO₂ CH₃ SC₆H₅ 3098 —(CH₂)₅— NO₂ CH₃ SC₆H₅ 3099 H H CN CH₃ SC₆H₅ 3100 CH₃ CH₃ CN CH₃ SC₆H₅ 3101 CH₂CH₃ CH₂CH₃ CN CH₃ SC₆H₅ 3102 CH₂CH₂CH₃ CH₂CH₂CH₃ CN CH₃ SC₆H₅ 3103 OCH₃ OCH₃ CN CH₃ SC₆H₅ 3104 OCH₂CH₃ OCH₂CH₃ CN CH₃ SC₆H₅ 3105 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CN CH₃ SC₆H₅ 3106 SCH₃ SCH₃ CN CH₃ SC₆H₅ 3107 SCH₂CH₃ SCH₂CH₃ CN CH₃ SC₆H₅ 3108 N(CH₃)₂ N(CH₃)₂ CN CH₃ SC₆H₅ 3109 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CN CH₃ SC₆H₅ 3110 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CN CH₃ SC₆H₅ 3111 O—(CH₂CH₂)—O CN CH₃ SC₆H₅ 3112 O—(CH₂CH₂CH₂)—O CN CH₃ SC₆H₅ 3113 S—(CH₂CH₂)—S CN CH₃ SC₆H₅ 3114 S—(CH₂CH₂CH₂)—S CN CH₃ SC₆H₅ 3115 —(CH₂)₄— CN CH₃ SC₆H₅ 3116 —(CH₂)₅— CN CH₃ SC₆H₅ 3117 H H F CH₃ SC₆H₅ 3118 CH₃ CH₃ F CH₃ SC₆H₅ 3119 CH₂CH₃ CH₂CH₃ F CH₃ SC₆H₅ 3120 CH₂CH₂CH₃ CH₂CH₂CH₃ F CH₃ SC₆H₅ 3121 OCH₃ OCH₃ F CH₃ SC₆H₅ 3122 OCH₂CH₃ OCH₂CH₃ F CH₃ SC₆H₅ 3123 OCH₂CH₂CH₃ OCH₂CH₂CH₃ F CH₃ SC₆H₅ 3124 SCH₃ SCH₃ F CH₃ SC₆H₅ 3125 SCH₂CH₃ SCH₂CH₃ F CH₃ SC₆H₅ 3126 N(CH₃)₂ N(CH₃)₂ F CH₃ SC₆H₅ 3127 N(CH₂CH₃)₂ N(CH₂CH₃)₂ F CH₃ SC₆H₅ 3128 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) F CH₃ SC₆H₅ 3129 O—(CH₂CH₂)—O F CH₃ SC₆H₅ 3130 O—(CH₂CH₂CH₂)—O F CH₃ SC₆H₅ 3131 S—(CH₂CH₂)—S F CH₃ SC₆H₅ 3132 S—(CH₂CH₂CH₂)—S F CH₃ SC₆H₅ 3133 —(CH₂)₄— F CH₃ SC₆H₅ 3134 —(CH₂)₅— F CH₃ SC₆H₅ 3135 H H Cl CH₃ SC₆H₅ 3136 CH₃ CH₃ Cl CH₃ SC₆H₅ 3137 CH₂CH₃ CH₂CH₃ Cl CH₃ SC₆H₅ 3138 CH₂CH₂CH₃ CH₂CH₂CH₃ Cl CH₃ SC₆H₅ 3139 OCH₃ OCH₃ Cl CH₃ SC₆H₅ 3140 OCH₂CH₃ OCH₂CH₃ Cl CH₃ SC₆H₅ 3141 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Cl CH₃ SC₆H₅ 3142 SCH₃ SCH₃ Cl CH₃ SC₆H₅ 3143 SCH₂CH₃ SCH₂CH₃ Cl CH₃ SC₆H₅ 3144 N(CH₃)₂ N(CH₃)₂ Cl CH₃ SC₆H₅ 3145 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Cl CH₃ SC₆H₅ 3146 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Cl CH₃ SC₆H₅ 3147 O—(CH₂CH₂)—O Cl CH₃ SC₆H₅ 3148 O—(CH₂CH₂CH₂)—O Cl CH₃ SC₆H₅ 3149 S—(CH₂CH₂)—S Cl CH₃ SC₆H₅ 3150 S—(CH₂CH₂CH₂)—S Cl CH₃ SC₆H₅ 3151 —(CH₂)₄— Cl CH₃ SC₆H₅ 3152 —(CH₂)₅— Cl CH₃ SC₆H₅ 3153 H H Br CH₃ SC₆H₅ 3154 CH₃ CH₃ Br CH₃ SC₆H₅ 3155 CH₂CH₃ CH₂CH₃ Br CH₃ SC₆H₅ 3156 CH₂CH₂CH₃ CH₂CH₂CH₃ Br CH₃ SC₆H₅ 3157 OCH₃ OCH₃ Br CH₃ SC₆H₅ 3158 OCH₂CH₃ OCH₂CH₃ Br CH₃ SC₆H₅ 3159 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Br CH₃ SC₆H₅ 3160 SCH₃ SCH₃ Br CH₃ SC₆H₅ 3161 SCH₂CH₃ SCH₂CH₃ Br CH₃ SC₆H₅ 3162 N(CH₃)₂ N(CH₃)₂ Br CH₃ SC₆H₅ 3163 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Br CH₃ SC₆H₅ 3164 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Br CH₃ SC₆H₅ 3165 O—(CH₂CH₂)—O Br CH₃ SC₆H₅ 3166 O—(CH₂CH₂CH₂)—O Br CH₃ SC₆H₅ 3167 S—(CH₂CH₂)—S Br CH₃ SC₆H₅ 3168 S—(CH₂CH₂CH₂)—S Br CH₃ SC₆H₅ 3169 —(CH₂)₄— Br CH₃ SC₆H₅ 3170 —(CH₂)₅— Br CH₃ SC₆H₅ 3171 H H CH₃ CH₃ SC₆H₅ 3172 CH₃ CH₃ CH₃ CH₃ SC₆H₅ 3173 CH₂CH₃ CH₂CH₃ CH₃ CH₃ SC₆H₅ 3174 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₃ CH₃ SC₆H₅ 3175 OCH₃ OCH₃ CH₃ CH₃ SC₆H₅ 3176 OCH₂CH₃ OCH₂CH₃ CH₃ CH₃ SC₆H₅ 3177 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₃ CH₃ SC₆H₅ 3178 SCH₃ SCH₃ CH₃ CH₃ SC₆H₅ 3179 SCH₂CH₃ SCH₂CH₃ CH₃ CH₃ SC₆H₅ 3180 N(CH₃)₂ N(CH₃)₂ CH₃ CH₃ SC₆H₅ 3181 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₃ CH₃ SC₆H₅ 3182 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₃ CH₃ SC₆H₅ 3183 O—(CH₂CH₂)—O CH₃ CH₃ SC₆H₅ 3184 O—(CH₂CH₂CH₂)—O CH₃ CH₃ SC₆H₅ 3185 S—(CH₂CH₂)—S CH₃ CH₃ SC₆H₅ 3186 S—(CH₂CH₂CH₂)—S CH₃ CH₃ SC₆H₅ 3187 —(CH₂)₄— CH₃ CH₃ SC₆H₅ 3188 —(CH₂)₅— CH₃ CH₃ SC₆H₅ 3189 H H CH₂CH₃ CH₃ SC₆H₅ 3190 CH₃ CH₃ CH₂CH₃ CH₃ SC₆H₅ 3191 CH₂CH₃ CH₂CH₃ CH₂CH₃ CH₃ SC₆H₅ 3192 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₂CH₃ CH₃ SC₆H₅ 3193 OCH₃ OCH₃ CH₂CH₃ CH₃ SC₆H₅ 3194 OCH₂CH₃ OCH₂CH₃ CH₂CH₃ CH₃ SC₆H₅ 3195 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₂CH₃ CH₃ SC₆H₅ 3196 SCH₃ SCH₃ CH₂CH₃ CH₃ SC₆H₅ 3197 SCH₂CH₃ SCH₂CH₃ CH₂CH₃ CH₃ SC₆H₅ 3198 N(CH₃)₂ N(CH₃)₂ CH₂CH₃ CH₃ SC₆H₅ 3199 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₂CH₃ CH₃ SC₆H₅ 3200 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₂CH₃ CH₃ SC₆H₅ 3201 O—(CH₂CH₂)—O CH₂CH₃ CH₃ SC₆H₅ 3202 O—(CH₂CH₂CH₂)—O CH₂CH₃ CH₃ SC₆H₅ 3203 S—(CH₂CH₂)—S CH₂CH₃ CH₃ SC₆H₅ 3204 S—(CH₂CH₂CH₂)—S CH₂CH₃ CH₃ SC₆H₅ 3205 —(CH₂)₄— CH₂CH₃ CH₃ SC₆H₅ 3206 —(CH₂)₅— CH₂CH₃ CH₃ SC₆H₅ 3207 H H CF₃ CH₃ SC₆H₅ 3208 CH₃ CH₃ CF₃ CH₃ SC₆H₅ 3209 CH₂CH₃ CH₂CH₃ CF₃ CH₃ SC₆H₅ 3210 CH₂CH₂CH₃ CH₂CH₂CH₃ CF₃ CH₃ SC₆H₅ 3211 OCH₃ OCH₃ CF₃ CH₃ SC₆H₅ 3212 OCH₂CH₃ OCH₂CH₃ CF₃ CH₃ SC₆H₅ 3213 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CF₃ CH₃ SC₆H₅ 3214 SCH₃ SCH₃ CF₃ CH₃ SC₆H₅ 3215 SCH₂CH₃ SCH₂CH₃ CF₃ CH₃ SC₆H₅ 3216 N(CH₃)₂ N(CH₃)₂ CF₃ CH₃ SC₆H₅ 3217 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CF₃ CH₃ SC₆H₅ 3218 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CF₃ CH₃ SC₆H₅ 3219 O—(CH₂CH₂)—O CF₃ CH₃ SC₆H₅ 3220 O—(CH₂CH₂CH₂)—O CF₃ CH₃ SC₆H₅ 3221 S—(CH₂CH₂)—S CF₃ CH₃ SC₆H₅ 3222 S—(CH₂CH₂CH₂)—S CF₃ CH₃ SC₆H₅ 3223 —(CH₂)₄— CF₃ CH₃ SC₆H₅ 3224 —(CH₂)₅— CF₃ CH₃ SC₆H₅ 3225 H H OCH₃ CH₃ SC₆H₅ 3226 CH₃ CH₃ OCH₃ CH₃ SC₆H₅ 3227 CH₂CH₃ CH₂CH₃ OCH₃ CH₃ SC₆H₅ 3228 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₃ CH₃ SC₆H₅ 3229 OCH₃ OCH₃ OCH₃ CH₃ SC₆H₅ 3230 OCH₂CH₃ OCH₂CH₃ OCH₃ CH₃ SC₆H₅ 3231 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₃ CH₃ SC₆H₅ 3232 SCH₃ SCH₃ OCH₃ CH₃ SC₆H₅ 3233 SCH₂CH₃ SCH₂CH₃ OCH₃ CH₃ SC₆H₅ 3234 N(CH₃)₂ N(CH₃)₂ OCH₃ CH₃ SC₆H₅ 3235 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₃ CH₃ SC₆H₅ 3236 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₃ CH₃ SC₆H₅ 3237 O—(CH₂CH₂)—O OCH₃ CH₃ SC₆H₅ 3238 O—(CH₂CH₂CH₂)—O OCH₃ CH₃ SC₆H₅ 3239 S—(CH₂CH₂)—S OCH₃ CH₃ SC₆H₅ 3240 S—(CH₂CH₂CH₂)—S OCH₃ CH₃ SC₆H₅ 3241 —(CH₂)₄— OCH₃ CH₃ SC₆H₅ 3242 —(CH₂)₅— OCH₃ CH₃ SC₆H₅ 3243 H H OCH₂CH₃ CH₃ SC₆H₅ 3244 CH₃ CH₃ OCH₂CH₃ CH₃ SC₆H₅ 3245 CH₂CH₃ CH₂CH₃ OCH₂CH₃ CH₃ SC₆H₅ 3246 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₂CH₃ CH₃ SC₆H₅ 3247 OCH₃ OCH₃ OCH₂CH₃ CH₃ SC₆H₅ 3248 OCH₂CH₃ OCH₂CH₃ OCH₂CH₃ CH₃ SC₆H₅ 3249 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₂CH₃ CH₃ SC₆H₅ 3250 SCH₃ SCH₃ OCH₂CH₃ CH₃ SC₆H₅ 3251 SCH₂CH₃ SCH₂CH₃ OCH₂CH₃ CH₃ SC₆H₅ 3252 N(CH₃)₂ N(CH₃)₂ OCH₂CH₃ CH₃ SC₆H₅ 3253 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₂CH₃ CH₃ SC₆H₅ 3254 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₂CH₃ CH₃ SC₆H₅ 3255 O—(CH₂CH₂)—O OCH₂CH₃ CH₃ SC₆H₅ 3256 O—(CH₂CH₂CH₂)—O OCH₂CH₃ CH₃ SC₆H₅ 3257 S—(CH₂CH₂)—S OCH₂CH₃ CH₃ SC₆H₅ 3258 S—(CH₂CH₂CH₂)—S OCH₂CH₃ CH₃ SC₆H₅ 3259 —(CH₂)₄— OCH₂CH₃ CH₃ SC₆H₅ 3260 —(CH₂)₅— OCH₂CH₃ CH₃ SC₆H₅ 3261 H H SCH₃ CH₃ SC₆H₅ 3262 CH₃ CH₃ SCH₃ CH₃ SC₆H₅ 3263 CH₂CH₃ CH₂CH₃ SCH₃ CH₃ SC₆H₅ 3264 CH₂CH₂CH₃ CH₂CH₂CH₃ SCH₃ CH₃ SC₆H₅ 3265 OCH₃ OCH₃ SCH₃ CH₃ SC₆H₅ 3266 OCH₂CH₃ OCH₂CH₃ SCH₃ CH₃ SC₆H₅ 3267 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SCH₃ CH₃ SC₆H₅ 3268 SCH₃ SCH₃ SCH₃ CH₃ SC₆H₅ 3269 SCH₂CH₃ SCH₂CH₃ SCH₃ CH₃ SC₆H₅ 3270 N(CH₃)₂ N(CH₃)₂ SCH₃ CH₃ SC₆H₅ 3271 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SCH₃ CH₃ SC₆H₅ 3272 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SCH₃ CH₃ SC₆H₅ 3273 O—(CH₂CH₂)—O SCH₃ CH₃ SC₆H₅ 3274 O—(CH₂CH₂CH₂)—O SCH₃ CH₃ SC₆H₅ 3275 S—(CH₂CH₂)—S SCH₃ CH₃ SC₆H₅ 3276 S—(CH₂CH₂CH₂)—S SCH₃ CH₃ SC₆H₅ 3277 —(CH₂)₄— SCH₃ CH₃ SC₆H₅ 3278 —(CH₂)₅— SCH₃ CH₃ SC₆H₅ 3279 H H SO₂CH₃ CH₃ SC₆H₅ 3280 CH₃ CH₃ SO₂CH₃ CH₃ SC₆H₅ 3281 CH₂CH₃ CH₂CH₃ SO₂CH₃ CH₃ SC₆H₅ 3282 CH₂CH₂CH₃ CH₂CH₂CH₃ SO₂CH₃ CH₃ SC₆H₅ 3283 OCH₃ OCH₃ SO₂CH₃ CH₃ SC₆H₅ 3284 OCH₂CH₃ OCH₂CH₃ SO₂CH₃ CH₃ SC₆H₅ 3285 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SO₂CH₃ CH₃ SC₆H₅ 3286 SCH₃ SCH₃ SO₂CH₃ CH₃ SC₆H₅ 3287 SCH₂CH₃ SCH₂CH₃ SO₂CH₃ CH₃ SC₆H₅ 3288 N(CH₃)₂ N(CH₃)₂ SO₂CH₃ CH₃ SC₆H₅ 3289 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SO₂CH₃ CH₃ SC₆H₅ 3290 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SO₂CH₃ CH₃ SC₆H₅ 3291 O—(CH₂CH₂)—O SO₂CH₃ CH₃ SC₆H₅ 3292 O—(CH₂CH₂CH₂)—O SO₂CH₃ CH₃ SC₆H₅ 3293 S—(CH₂CH₂)—S SO₂CH₃ CH₃ SC₆H₅ 3294 S—(CH₂CH₂CH₂)—S SO₂CH₃ CH₃ SC₆H₅ 3295 —(CH₂)₄— SO₂CH₃ CH₃ SC₆H₅ 3296 —(CH₂)₅— SO₂CH₃ CH₃ SC₆H₅ 3297 H H PO(OCH₃)₂ CH₃ SC₆H₅ 3298 CH₃ CH₃ PO(OCH₃)₂ CH₃ SC₆H₅ 3299 CH₂CH₃ CH₂CH₃ PO(OCH₃)₂ CH₃ SC₆H₅ 3300 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₃)₂ CH₃ SC₆H₅ 3301 OCH₃ OCH₃ PO(OCH₃)₂ CH₃ SC₆H₅ 3302 OCH₂CH₃ OCH₂CH₃ PO(OCH₃)₂ CH₃ SC₆H₅ 3303 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₃)₂ CH₃ SC₆H₅ 3304 SCH₃ SCH₃ PO(OCH₃)₂ CH₃ SC₆H₅ 3305 SCH₂CH₃ SCH₂CH₃ PO(OCH₃)₂ CH₃ SC₆H₅ 3306 N(CH₃)₂ N(CH₃)₂ PO(OCH₃)₂ CH₃ SC₆H₅ 3307 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₃)₂ CH₃ SC₆H₅ 3308 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₃)₂ CH₃ SC₆H₅ 3309 O—(CH₂CH₂)—O PO(OCH₃)₂ CH₃ SC₆H₅ 3310 O—(CH₂CH₂CH₂)—O PO(OCH₃)₂ CH₃ SC₆H₅ 3311 S—(CH₂CH₂)—S PO(OCH₃)₂ CH₃ SC₆H₅ 3312 S—(CH₂CH₂CH₂)—S PO(OCH₃)₂ CH₃ SC₆H₅ 3313 —(CH₂)₄— PO(OCH₃)₂ CH₃ SC₆H₅ 3314 —(CH₂)₅— PO(OCH₃)₂ CH₃ SC₆H₅ 3315 H H PO(OCH₂CH₃)₂ CH₃ SC₆H₅ 3316 CH₃ CH₃ PO(OCH₂CH₃)₂ CH₃ SC₆H₅ 3317 CH₂CH₃ CH₂CH₃ PO(OCH₂CH₃)₂ CH₃ SC₆H₅ 3318 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₂CH₃)₂ CH₃ SC₆H₅ 3319 OCH₃ OCH₃ PO(OCH₂CH₃)₂ CH₃ SC₆H₅ 3320 OCH₂CH₃ OCH₂CH₃ PO(OCH₂CH₃)₂ CH₃ SC₆H₅ 3321 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₂CH₃)₂ CH₃ SC₆H₅ 3322 SCH₃ SCH₃ PO(OCH₂CH₃)₂ CH₃ SC₆H₅ 3323 SCH₂CH₃ SCH₂CH₃ PO(OCH₂CH₃)₂ CH₃ SC₆H₅ 3324 N(CH₃)₂ N(CH₃)₂ PO(OCH₂CH₃)₂ CH₃ SC₆H₅ 3325 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₂CH₃)₂ CH₃ SC₆H₅ 3326 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₂CH₃)₂ CH₃ SC₆H₅ 3327 O—(CH₂CH₂)—O PO(OCH₂CH₃)₂ CH₃ SC₆H₅ 3328 O—(CH₂CH₂CH₂)—O PO(OCH₂CH₃)₂ CH₃ SC₆H₅ 3329 S—(CH₂CH₂)—S PO(OCH₂CH₃)₂ CH₃ SC₆H₅ 3330 S—(CH₂CH₂CH₂)—S PO(OCH₂CH₃)₂ CH₃ SC₆H₅ 3331 —(CH₂)₄— PO(OCH₂CH₃)₂ CH₃ SC₆H₅ 3332 —(CH₂)₅— PO(OCH₂CH₃)₂ CH₃ SC₆H₅ 3333 H H PO(CH₃)₂ CH₃ SC₆H₅ 3334 CH₃ CH₃ PO(CH₃)₂ CH₃ SC₆H₅ 3335 CH₂CH₃ CH₂CH₃ PO(CH₃)₂ CH₃ SC₆H₅ 3336 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₃)₂ CH₃ SC₆H₅ 3337 OCH₃ OCH₃ PO(CH₃)₂ CH₃ SC₆H₅ 3338 OCH₂CH₃ OCH₂CH₃ PO(CH₃)₂ CH₃ SC₆H₅ 3339 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₃)₂ CH₃ SC₆H₅ 3340 SCH₃ SCH₃ PO(CH₃)₂ CH₃ SC₆H₅ 3341 SCH₂CH₃ SCH₂CH₃ PO(CH₃)₂ CH₃ SC₆H₅ 3342 N(CH₃)₂ N(CH₃)₂ PO(CH₃)₂ CH₃ SC₆H₅ 3343 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₃)₂ CH₃ SC₆H₅ 3344 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₃)₂ CH₃ SC₆H₅ 3345 O—(CH₂CH₂)—O PO(CH₃)₂ CH₃ SC₆H₅ 3346 O—(CH₂CH₂CH₂)—O PO(CH₃)₂ CH₃ SC₆H₅ 3347 S—(CH₂CH₂)—S PO(CH₃)₂ CH₃ SC₆H₅ 3348 S—(CH₂CH₂CH₂)—S PO(CH₃)₂ CH₃ SC₆H₅ 3349 —(CH₂)₄— PO(CH₃)₂ CH₃ SC₆H₅ 3350 —(CH₂)₅— PO(CH₃)₂ CH₃ SC₆H₅ 3351 H H PO(CH₂CH₃)₂ CH₃ SC₆H₅ 3352 CH₃ CH₃ PO(CH₂CH₃)₂ CH₃ SC₆H₅ 3353 CH₂CH₃ CH₂CH₃ PO(CH₂CH₃)₂ CH₃ SC₆H₅ 3354 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₂CH₃)₂ CH₃ SC₆H₅ 3355 OCH₃ OCH₃ PO(CH₂CH₃)₂ CH₃ SC₆H₅ 3356 OCH₂CH₃ OCH₂CH₃ PO(CH₂CH₃)₂ CH₃ SC₆H₅ 3357 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₂CH₃)₂ CH₃ SC₆H₅ 3358 SCH₃ SCH₃ PO(CH₂CH₃)₂ CH₃ SC₆H₅ 3359 SCH₂CH₃ SCH₂CH₃ PO(CH₂CH₃)₂ CH₃ SC₆H₅ 3360 N(CH₃)₂ N(CH₃)₂ PO(CH₂CH₃)₂ CH₃ SC₆H₅ 3361 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₂CH₃)₂ CH₃ SC₆H₅ 3362 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₂CH₃)₂ CH₃ SC₆H₅ 3363 O—(CH₂CH₂)—O PO(CH₂CH₃)₂ CH₃ SC₆H₅ 3364 O—(CH₂CH₂CH₂)—O PO(CH₂CH₃)₂ CH₃ SC₆H₅ 3365 S—(CH₂CH₂)—S PO(CH₂CH₃)₂ CH₃ SC₆H₅ 3366 S—(CH₂CH₂CH₂)—S PO(CH₂CH₃)₂ CH₃ SC₆H₅ 3367 —(CH₂)₄— PO(CH₂CH₃)₂ CH₃ SC₆H₅ 3368 —(CH₂)₅— PO(CH₂CH₃)₂ CH₃ SC₆H₅ 3369 H H H CH₃ Het1 3370 CH₃ CH₃ H CH₃ Het1 3371 CH₂CH₃ CH₂CH₃ H CH₃ Het1 3372 CH₂CH₂CH₃ CH₂CH₂CH₃ H CH₃ Het1 3373 OCH₃ OCH₃ H CH₃ Het1 3374 OCH₂CH₃ OCH₂CH₃ H CH₃ Het1 3375 OCH₂CH₂CH₃ OCH₂CH₂CH₃ H CH₃ Het1 3376 SCH₃ SCH₃ H CH₃ Het1 3377 SCH₂CH₃ SCH₂CH₃ H CH₃ Het1 3378 N(CH₃)₂ N(CH₃)₂ H CH₃ Het1 3379 N(CH₂CH₃)₂ N(CH₂CH₃)₂ H CH₃ Het1 3380 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) H CH₃ Het1 3381 O—(CH₂CH₂)—O H CH₃ Het1 3382 O—(CH₂CH₂CH₂)—O H CH₃ Het1 3383 S—(CH₂CH₂)—S H CH₃ Het1 3384 S—(CH₂CH₂CH₂)—S H CH₃ Het1 3385 —(CH₂)₄— H CH₃ Het1 3386 —(CH₂)₅— H CH₃ Het1 3387 H H NO₂ CH₃ Het1 3388 CH₃ CH₃ NO₂ CH₃ Het1 3389 CH₂CH₃ CH₂CH₃ NO₂ CH₃ Het1 3390 CH₂CH₂CH₃ CH₂CH₂CH₃ NO₂ CH₃ Het1 3391 OCH₃ OCH₃ NO₂ CH₃ Het1 3392 OCH₂CH₃ OCH₂CH₃ NO₂ CH₃ Het1 3393 OCH₂CH₂CH₃ OCH₂CH₂CH₃ NO₂ CH₃ Het1 3394 SCH₃ SCH₃ NO₂ CH₃ Het1 3395 SCH₂CH₃ SCH₂CH₃ NO₂ CH₃ Het1 3396 N(CH₃)₂ N(CH₃)₂ NO₂ CH₃ Het1 3397 N(CH₂CH₃)₂ N(CH₂CH₃)₂ NO₂ CH₃ Het1 3398 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) NO₂ CH₃ Het1 3399 O—(CH₂CH₂)—O NO₂ CH₃ Het1 3400 O—(CH₂CH₂CH₂)—O NO₂ CH₃ Het1 3401 S—(CH₂CH₂)—S NO₂ CH₃ Het1 3402 S—(CH₂CH₂CH₂)—S NO₂ CH₃ Het1 3403 —(CH₂)₄— NO₂ CH₃ Het1 3404 —(CH₂)₅— NO₂ CH₃ Het1 3405 H H CN CH₃ Het1 3406 CH₃ CH₃ CN CH₃ Het1 3407 CH₂CH₃ CH₂CH₃ CN CH₃ Het1 3408 CH₂CH₂CH₃ CH₂CH₂CH₃ CN CH₃ Het1 3409 OCH₃ OCH₃ CN CH₃ Het1 3410 OCH₂CH₃ OCH₂CH₃ CN CH₃ Het1 3411 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CN CH₃ Het1 3412 SCH₃ SCH₃ CN CH₃ Het1 3413 SCH₂CH₃ SCH₂CH₃ CN CH₃ Het1 3414 N(CH₃)₂ N(CH₃)₂ CN CH₃ Het1 3415 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CN CH₃ Het1 3416 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CN CH₃ Het1 3417 O—(CH₂CH₂)—O CN CH₃ Het1 3418 O—(CH₂CH₂CH₂)—O CN CH₃ Het1 3419 S—(CH₂CH₂)—S CN CH₃ Het1 3420 S—(CH₂CH₂CH₂)—S CN CH₃ Het1 3421 —(CH₂)₄— CN CH₃ Het1 3422 —(CH₂)₅— CN CH₃ Het1 3423 H H F CH₃ Het1 3424 CH₃ CH₃ F CH₃ Het1 3425 CH₂CH₃ CH₂CH₃ F CH₃ Het1 3426 CH₂CH₂CH₃ CH₂CH₂CH₃ F CH₃ Het1 3427 OCH₃ OCH₃ F CH₃ Het1 3428 OCH₂CH₃ OCH₂CH₃ F CH₃ Het1 3429 OCH₂CH₂CH₃ OCH₂CH₂CH₃ F CH₃ Het1 3430 SCH₃ SCH₃ F CH₃ Het1 3431 SCH₂CH₃ SCH₂CH₃ F CH₃ Het1 3432 N(CH₃)₂ N(CH₃)₂ F CH₃ Het1 3433 N(CH₂CH₃)₂ N(CH₂CH₃)₂ F CH₃ Het1 3434 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) F CH₃ Het1 3435 O—(CH₂CH₂)—O F CH₃ Het1 3436 O—(CH₂CH₂CH₂)—O F CH₃ Het1 3437 S—(CH₂CH₂)—S F CH₃ Het1 3438 S—(CH₂CH₂CH₂)—S F CH₃ Het1 3439 —(CH₂)₄— F CH₃ Het1 3440 —(CH₂)₅— F CH₃ Het1 3441 H H Cl CH₃ Het1 3442 CH₃ CH₃ Cl CH₃ Het1 3443 CH₂CH₃ CH₂CH₃ Cl CH₃ Het1 3444 CH₂CH₂CH₃ CH₂CH₂CH₃ Cl CH₃ Het1 3445 OCH₃ OCH₃ Cl CH₃ Het1 3446 OCH₂CH₃ OCH₂CH₃ Cl CH₃ Het1 3447 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Cl CH₃ Het1 3448 SCH₃ SCH₃ Cl CH₃ Het1 3449 SCH₂CH₃ SCH₂CH₃ Cl CH₃ Het1 3450 N(CH₃)₂ N(CH₃)₂ Cl CH₃ Het1 3451 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Cl CH₃ Het1 3452 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Cl CH₃ Het1 3453 O—(CH₂CH₂)—O Cl CH₃ Het1 3454 O—(CH₂CH₂CH₂)—O Cl CH₃ Het1 3455 S—(CH₂CH₂)—S Cl CH₃ Het1 3456 S—(CH₂CH₂CH₂)—S Cl CH₃ Het1 3457 —(CH₂)₄— Cl CH₃ Het1 3458 —(CH₂)₅— Cl CH₃ Het1 3459 H H Br CH₃ Het1 3460 CH₃ CH₃ Br CH₃ Het1 3461 CH₂CH₃ CH₂CH₃ Br CH₃ Het1 3462 CH₂CH₂CH₃ CH₂CH₂CH₃ Br CH₃ Het1 3463 OCH₃ OCH₃ Br CH₃ Het1 3464 OCH₂CH₃ OCH₂CH₃ Br CH₃ Het1 3465 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Br CH₃ Het1 3466 SCH₃ SCH₃ Br CH₃ Het1 3467 SCH₂CH₃ SCH₂CH₃ Br CH₃ Het1 3468 N(CH₃)₂ N(CH₃)₂ Br CH₃ Het1 3469 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Br CH₃ Het1 3470 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Br CH₃ Het1 3471 O—(CH₂CH₂)—O Br CH₃ Het1 3472 O—(CH₂CH₂CH₂)—O Br CH₃ Het1 3473 S—(CH₂CH₂)—S Br CH₃ Het1 3474 S—(CH₂CH₂CH₂)—S Br CH₃ Het1 3475 —(CH₂)₄— Br CH₃ Het1 3476 —(CH₂)₅— Br CH₃ Het1 3477 H H CH₃ CH₃ Het1 3478 CH₃ CH₃ CH₃ CH₃ Het1 3479 CH₂CH₃ CH₂CH₃ CH₃ CH₃ Het1 3480 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₃ CH₃ Het1 3481 OCH₃ OCH₃ CH₃ CH₃ Het1 3482 OCH₂CH₃ OCH₂CH₃ CH₃ CH₃ Het1 3483 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₃ CH₃ Het1 3484 SCH₃ SCH₃ CH₃ CH₃ Het1 3485 SCH₂CH₃ SCH₂CH₃ CH₃ CH₃ Het1 3486 N(CH₃)₂ N(CH₃)₂ CH₃ CH₃ Het1 3487 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₃ CH₃ Het1 3488 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₃ CH₃ Het1 3489 O—(CH₂CH₂)—O CH₃ CH₃ Het1 3490 O—(CH₂CH₂CH₂)—O CH₃ CH₃ Het1 3491 S—(CH₂CH₂)—S CH₃ CH₃ Het1 3492 S—(CH₂CH₂CH₂)—S CH₃ CH₃ Het1 3493 —(CH₂)₄— CH₃ CH₃ Het1 3494 —(CH₂)₅— CH₃ CH₃ Het1 3495 H H CH₂CH₃ CH₃ Het1 3496 CH₃ CH₃ CH₂CH₃ CH₃ Het1 3497 CH₂CH₃ CH₂CH₃ CH₂CH₃ CH₃ Het1 3498 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₂CH₃ CH₃ Het1 3499 OCH₃ OCH₃ CH₂CH₃ CH₃ Het1 3500 OCH₂CH₃ OCH₂CH₃ CH₂CH₃ CH₃ Het1 3501 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₂CH₃ CH₃ Het1 3502 SCH₃ SCH₃ CH₂CH₃ CH₃ Het1 3503 SCH₂CH₃ SCH₂CH₃ CH₂CH₃ CH₃ Het1 3504 N(CH₃)₂ N(CH₃)₂ CH₂CH₃ CH₃ Het1 3505 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₂CH₃ CH₃ Het1 3506 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₂CH₃ CH₃ Het1 3507 O—(CH₂CH₂)—O CH₂CH₃ CH₃ Het1 3508 O—(CH₂CH₂CH₂)—O CH₂CH₃ CH₃ Het1 3509 S—(CH₂CH₂)—S CH₂CH₃ CH₃ Het1 3510 S—(CH₂CH₂CH₂)—S CH₂CH₃ CH₃ Het1 3511 —(CH₂)₄— CH₂CH₃ CH₃ Het1 3512 —(CH₂)₅— CH₂CH₃ CH₃ Het1 3513 H H CF₃ CH₃ Het1 3514 CH₃ CH₃ CF₃ CH₃ Het1 3515 CH₂CH₃ CH₂CH₃ CF₃ CH₃ Het1 3516 CH₂CH₂CH₃ CH₂CH₂CH₃ CF₃ CH₃ Het1 3517 OCH₃ OCH₃ CF₃ CH₃ Het1 3518 OCH₂CH₃ OCH₂CH₃ CF₃ CH₃ Het1 3519 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CF₃ CH₃ Het1 3520 SCH₃ SCH₃ CF₃ CH₃ Het1 3521 SCH₂CH₃ SCH₂CH₃ CF₃ CH₃ Het1 3522 N(CH₃)₂ N(CH₃)₂ CF₃ CH₃ Het1 3523 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CF₃ CH₃ Het1 3524 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CF₃ CH₃ Het1 3525 O—(CH₂CH₂)—O CF₃ CH₃ Het1 3526 O—(CH₂CH₂CH₂)—O CF₃ CH₃ Het1 3527 S—(CH₂CH₂)—S CF₃ CH₃ Het1 3528 S—(CH₂CH₂CH₂)—S CF₃ CH₃ Het1 3529 —(CH₂)₄— CF₃ CH₃ Het1 3530 —(CH₂)₅— CF₃ CH₃ Het1 3531 H H OCH₃ CH₃ Het1 3532 CH₃ CH₃ OCH₃ CH₃ Het1 3533 CH₂CH₃ CH₂CH₃ OCH₃ CH₃ Het1 3534 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₃ CH₃ Het1 3535 OCH₃ OCH₃ OCH₃ CH₃ Het1 3536 OCH₂CH₃ OCH₂CH₃ OCH₃ CH₃ Het1 3537 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₃ CH₃ Het1 3538 SCH₃ SCH₃ OCH₃ CH₃ Het1 3539 SCH₂CH₃ SCH₂CH₃ OCH₃ CH₃ Het1 3540 N(CH₃)₂ N(CH₃)₂ OCH₃ CH₃ Het1 3541 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₃ CH₃ Het1 3542 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₃ CH₃ Het1 3543 O—(CH₂CH₂)—O OCH₃ CH₃ Het1 3544 O—(CH₂CH₂CH₂)—O OCH₃ CH₃ Het1 3545 S—(CH₂CH₂)—S OCH₃ CH₃ Het1 3546 S—(CH₂CH₂CH₂)—S OCH₃ CH₃ Het1 4044 N(CH₃)₂ N(CH₃)₂ F CH₃ Het3 4045 N(CH₂CH₃)₂ N(CH₂CH₃)₂ F CH₃ Het3 4046 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) F CH₃ Het3 4047 O—(CH₂CH₂)—O F CH₃ Het3 4048 O—(CH₂CH₂CH₂)—O F CH₃ Het3 4049 S—(CH₂CH₂)—S F CH₃ Het3 4050 S—(CH₂CH₂CH₂)—S F CH₃ Het3 4051 —(CH₂)₄— F CH₃ Het3 4052 —(CH₂)₅— F CH₃ Het3 4053 H H Cl CH₃ Het3 4054 CH₃ CH₃ Cl CH₃ Het3 4055 CH₂CH₃ CH₂CH₃ Cl CH₃ Het3 4056 CH₂CH₂CH₃ CH₂CH₂CH₃ Cl CH₃ Het3 4057 OCH₃ OCH₃ Cl CH₃ Het3 4058 OCH₂CH₃ OCH₂CH₃ Cl CH₃ Het3 4059 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Cl CH₃ Het3 4060 SCH₃ SCH₃ Cl CH₃ Het3 4061 SCH₂CH₃ SCH₂CH₃ Cl CH₃ Het3 4062 N(CH₃)₂ N(CH₃)₂ Cl CH₃ Het3 4063 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Cl CH₃ Het3 4064 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Cl CH₃ Het3 4065 O—(CH₂CH₂)—O Cl CH₃ Het3 4066 O—(CH₂CH₂CH₂)—O Cl CH₃ Het3 4067 S—(CH₂CH₂)—S Cl CH₃ Het3 4068 S—(CH₂CH₂CH₂)—S Cl CH₃ Het3 4069 —(CH₂)₄— Cl CH₃ Het3 4070 —(CH₂)₅— Cl CH₃ Het3 4071 H H Br CH₃ Het3 4072 CH₃ CH₃ Br CH₃ Het3 4073 CH₂CH₃ CH₂CH₃ Br CH₃ Het3 4074 CH₂CH₂CH₃ CH₂CH₂CH₃ Br CH₃ Het3 4075 OCH₃ OCH₃ Br CH₃ Het3 4076 OCH₂CH₃ OCH₂CH₃ Br CH₃ Het3 4077 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Br CH₃ Het3 4078 SCH₃ SCH₃ Br CH₃ Het3 4079 SCH₂CH₃ SCH₂CH₃ Br CH₃ Het3 4080 N(CH₃)₂ N(CH₃)₂ Br CH₃ Het3 4081 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Br CH₃ Het3 4082 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Br CH₃ Het3 4083 O—(CH₂CH₂)—O Br CH₃ Het3 4084 O—(CH₂CH₂CH₂)—O Br CH₃ Het3 4085 S—(CH₂CH₂)—S Br CH₃ Het3 4086 S—(CH₂CH₂CH₂)—S Br CH₃ Het3 4087 —(CH₂)₄— Br CH₃ Het3 4088 —(CH₂)₅— Br CH₃ Het3 4089 H H CH₃ CH₃ Het3 4090 CH₃ CH₃ CH₃ CH₃ Het3 4091 CH₂CH₃ CH₂CH₃ CH₃ CH₃ Het3 4092 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₃ CH₃ Het3 4093 OCH₃ OCH₃ CH₃ CH₃ Het3 4094 OCH₂CH₃ OCH₂CH₃ CH₃ CH₃ Het3 4095 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₃ CH₃ Het3 4096 SCH₃ SCH₃ CH₃ CH₃ Het3 4097 SCH₂CH₃ SCH₂CH₃ CH₃ CH₃ Het3 4098 N(CH₃)₂ N(CH₃)₂ CH₃ CH₃ Het3 4099 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₃ CH₃ Het3 4100 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₃ CH₃ Het3 4101 O—(CH₂CH₂)—O CH₃ CH₃ Het3 4102 O—(CH₂CH₂CH₂)—O CH₃ CH₃ Het3 4103 S—(CH₂CH₂)—S CH₃ CH₃ Het3 4104 S—(CH₂CH₂CH₂)—S CH₃ CH₃ Het3 4105 —(CH₂)₄— CH₃ CH₃ Het3 4106 —(CH₂)₅— CH₃ CH₃ Het3 4107 H H CH₂CH₃ CH₃ Het3 4108 CH₃ CH₃ CH₂CH₃ CH₃ Het3 4109 CH₂CH₃ CH₂CH₃ CH₂CH₃ CH₃ Het3 4110 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₂CH₃ CH₃ Het3 4111 OCH₃ OCH₃ CH₂CH₃ CH₃ Het3 4112 OCH₂CH₃ OCH₂CH₃ CH₂CH₃ CH₃ Het3 4113 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₂CH₃ CH₃ Het3 4114 SCH₃ SCH₃ CH₂CH₃ CH₃ Het3 4115 SCH₂CH₃ SCH₂CH₃ CH₂CH₃ CH₃ Het3 4116 N(CH₃)₂ N(CH₃)₂ CH₂CH₃ CH₃ Het3 4117 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₂CH₃ CH₃ Het3 4118 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₂CH₃ CH₃ Het3 4119 O—(CH₂CH₂)—O CH₂CH₃ CH₃ Het3 4120 O—(CH₂CH₂CH₂)—O CH₂CH₃ CH₃ Het3 4121 S—(CH₂CH₂)—S CH₂CH₃ CH₃ Het3 4122 S—(CH₂CH₂CH₂)—S CH₂CH₃ CH₃ Het3 4123 —(CH₂)₄— CH₂CH₃ CH₃ Het3 4124 —(CH₂)₅— CH₂CH₃ CH₃ Het3 4125 H H CF₃ CH₃ Het3 4126 CH₃ CH₃ CF₃ CH₃ Het3 4127 CH₂CH₃ CH₂CH₃ CF₃ CH₃ Het3 4128 CH₂CH₂CH₃ CH₂CH₂CH₃ CF₃ CH₃ Het3 4129 OCH₃ OCH₃ CF₃ CH₃ Het3 4130 OCH₂CH₃ OCH₂CH₃ CF₃ CH₃ Het3 4131 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CF₃ CH₃ Het3 4132 SCH₃ SCH₃ CF₃ CH₃ Het3 4133 SCH₂CH₃ SCH₂CH₃ CF₃ CH₃ Het3 4134 N(CH₃)₂ N(CH₃)₂ CF₃ CH₃ Het3 4135 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CF₃ CH₃ Het3 4136 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CF₃ CH₃ Het3 4137 O—(CH₂CH₂)—O CF₃ CH₃ Het3 4138 O—(CH₂CH₂CH₂)—O CF₃ CH₃ Het3 4139 S—(CH₂CH₂)—S CF₃ CH₃ Het3 4140 S—(CH₂CH₂CH₂)—S CF₃ CH₃ Het3 4141 —(CH₂)₄— CF₃ CH₃ Het3 4142 —(CH₂)₅— CF₃ CH₃ Het3 4143 H H OCH₃ CH₃ Het3 4144 CH₃ CH₃ OCH₃ CH₃ Het3 4145 CH₂CH₃ CH₂CH₃ OCH₃ CH₃ Het3 4146 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₃ CH₃ Het3 4147 OCH₃ OCH₃ OCH₃ CH₃ Het3 4148 OCH₂CH₃ OCH₂CH₃ OCH₃ CH₃ Het3 4149 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₃ CH₃ Het3 4150 SCH₃ SCH₃ OCH₃ CH₃ Het3 4151 SCH₂CH₃ SCH₂CH₃ OCH₃ CH₃ Het3 4152 N(CH₃)₂ N(CH₃)₂ OCH₃ CH₃ Het3 4153 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₃ CH₃ Het3 4154 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₃ CH₃ Het3 4155 O—(CH₂CH₂)—O OCH₃ CH₃ Het3 4156 O—(CH₂CH₂CH₂)—O OCH₃ CH₃ Het3 4157 S—(CH₂CH₂)—S OCH₃ CH₃ Het3 4158 S—(CH₂CH₂CH₂)—S OCH₃ CH₃ Het3 4159 —(CH₂)₄— OCH₃ CH₃ Het3 4160 —(CH₂)₅— OCH₃ CH₃ Het3 4161 H H OCH₂CH₃ CH₃ Het3 4162 CH₃ CH₃ OCH₂CH₃ CH₃ Het3 4163 CH₂CH₃ CH₂CH₃ OCH₂CH₃ CH₃ Het3 4164 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₂CH₃ CH₃ Het3 4165 OCH₃ OCH₃ OCH₂CH₃ CH₃ Het3 4166 OCH₂CH₃ OCH₂CH₃ OCH₂CH₃ CH₃ Het3 4167 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₂CH₃ CH₃ Het3 4168 SCH₃ SCH₃ OCH₂CH₃ CH₃ Het3 4169 SCH₂CH₃ SCH₂CH₃ OCH₂CH₃ CH₃ Het3 4170 N(CH₃)₂ N(CH₃)₂ OCH₂CH₃ CH₃ Het3 4171 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₂CH₃ CH₃ Het3 4172 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₂CH₃ CH₃ Het3 4173 O—(CH₂CH₂)—O OCH₂CH₃ CH₃ Het3 4174 O—(CH₂CH₂CH₂)—O OCH₂CH₃ CH₃ Het3 4175 S—(CH₂CH₂)—S OCH₂CH₃ CH₃ Het3 4176 S—(CH₂CH₂CH₂)—S OCH₂CH₃ CH₃ Het3 4177 —(CH₂)₄— OCH₂CH₃ CH₃ Het3 4178 —(CH₂)₅— OCH₂CH₃ CH₃ Het3 4179 H H SCH₃ CH₃ Het3 4180 CH₃ CH₃ SCH₃ CH₃ Het3 4181 CH₂CH₃ CH₂CH₃ SCH₃ CH₃ Het3 4182 CH₂CH₂CH₃ CH₂CH₂CH₃ SCH₃ CH₃ Het3 4183 OCH₃ OCH₃ SCH₃ CH₃ Het3 4184 OCH₂CH₃ OCH₂CH₃ SCH₃ CH₃ Het3 4185 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SCH₃ CH₃ Het3 4186 SCH₃ SCH₃ SCH₃ CH₃ Het3 4187 SCH₂CH₃ SCH₂CH₃ SCH₃ CH₃ Het3 4188 N(CH₃)₂ N(CH₃)₂ SCH₃ CH₃ Het3 4189 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SCH₃ CH₃ Het3 4190 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SCH₃ CH₃ Het3 4191 O—(CH₂CH₂)—O SCH₃ CH₃ Het3 4192 O—(CH₂CH₂CH₂)—O SCH₃ CH₃ Het3 4193 S—(CH₂CH₂)—S SCH₃ CH₃ Het3 4194 S—(CH₂CH₂CH₂)—S SCH₃ CH₃ Het3 4195 —(CH₂)₄— SCH₃ CH₃ Het3 4196 —(CH₂)₅— SCH₃ CH₃ Het3 4197 H H SO₂CH₃ CH₃ Het3 4198 CH₃ CH₃ SO₂CH₃ CH₃ Het3 4199 CH₂CH₃ CH₂CH₃ SO₂CH₃ CH₃ Het3 4200 CH₂CH₂CH₃ CH₂CH₂CH₃ SO₂CH₃ CH₃ Het3 4201 OCH₃ OCH₃ SO₂CH₃ CH₃ Het3 4202 OCH₂CH₃ OCH₂CH₃ SO₂CH₃ CH₃ Het3 4203 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SO₂CH₃ CH₃ Het3 4204 SCH₃ SCH₃ SO₂CH₃ CH₃ Het3 4205 SCH₂CH₃ SCH₂CH₃ SO₂CH₃ CH₃ Het3 4206 N(CH₃)₂ N(CH₃)₂ SO₂CH₃ CH₃ Het3 4207 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SO₂CH₃ CH₃ Het3 4208 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SO₂CH₃ CH₃ Het3 4209 O—(CH₂CH₂)—O SO₂CH₃ CH₃ Het3 4210 O—(CH₂CH₂CH₂)—O SO₂CH₃ CH₃ Het3 4211 S—(CH₂CH₂)—S SO₂CH₃ CH₃ Het3 4212 S—(CH₂CH₂CH₂)—S SO₂CH₃ CH₃ Het3 4213 —(CH₂)₄— SO₂CH₃ CH₃ Het3 4214 —(CH₂)₅— SO₂CH₃ CH₃ Het3 4215 H H PO(OCH₃)₂ CH₃ Het3 4216 CH₃ CH₃ PO(OCH₃)₂ CH₃ Het3 4217 CH₂CH₃ CH₂CH₃ PO(OCH₃)₂ CH₃ Het3 4218 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₃)₂ CH₃ Het3 4219 OCH₃ OCH₃ PO(OCH₃)₂ CH₃ Het3 4220 OCH₂CH₃ OCH₂CH₃ PO(OCH₃)₂ CH₃ Het3 4221 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₃)₂ CH₃ Het3 4222 SCH₃ SCH₃ PO(OCH₃)₂ CH₃ Het3 4223 SCH₂CH₃ SCH₂CH₃ PO(OCH₃)₂ CH₃ Het3 4224 N(CH₃)₂ N(CH₃)₂ PO(OCH₃)₂ CH₃ Het3 4225 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₃)₂ CH₃ Het3 4226 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₃)₂ CH₃ Het3 4227 O—(CH₂CH₂)—O PO(OCH₃)₂ CH₃ Het3 4228 O—(CH₂CH₂CH₂)—O PO(OCH₃)₂ CH₃ Het3 4229 S—(CH₂CH₂)—S PO(OCH₃)₂ CH₃ Het3 4230 S—(CH₂CH₂CH₂)—S PO(OCH₃)₂ CH₃ Het3 4231 —(CH₂)₄— PO(OCH₃)₂ CH₃ Het3 4232 —(CH₂)₅— PO(OCH₃)₂ CH₃ Het3 4233 H H PO(OCH₂CH₃)₂ CH₃ Het3 4234 CH₃ CH₃ PO(OCH₂CH₃)₂ CH₃ Het3 4235 CH₂CH₃ CH₂CH₃ PO(OCH₂CH₃)₂ CH₃ Het3 4236 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₂CH₃)₂ CH₃ Het3 4237 OCH₃ OCH₃ PO(OCH₂CH₃)₂ CH₃ Het3 4238 OCH₂CH₃ OCH₂CH₃ PO(OCH₂CH₃)₂ CH₃ Het3 4239 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₂CH₃)₂ CH₃ Het3 4240 SCH₃ SCH₃ PO(OCH₂CH₃)₂ CH₃ Het3 4241 SCH₂CH₃ SCH₂CH₃ PO(OCH₂CH₃)₂ CH₃ Het3 4242 N(CH₃)₂ N(CH₃)₂ PO(OCH₂CH₃)₂ CH₃ Het3 4243 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₂CH₃)₂ CH₃ Het3 4244 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₂CH₃)₂ CH₃ Het3 4245 O—(CH₂CH₂)—O PO(OCH₂CH₃)₂ CH₃ Het3 4246 O—(CH₂CH₂CH₂)—O PO(OCH₂CH₃)₂ CH₃ Het3 4247 S—(CH₂CH₂)—S PO(OCH₂CH₃)₂ CH₃ Het3 4248 S—(CH₂CH₂CH₂)—S PO(OCH₂CH₃)₂ CH₃ Het3 4249 —(CH₂)₄— PO(OCH₂CH₃)₂ CH₃ Het3 4250 —(CH₂)₅— PO(OCH₂CH₃)₂ CH₃ Het3 4251 H H PO(CH₃)₂ CH₃ Het3 4252 CH₃ CH₃ PO(CH₃)₂ CH₃ Het3 4253 CH₂CH₃ CH₂CH₃ PO(CH₃)₂ CH₃ Het3 4254 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₃)₂ CH₃ Het3 4255 OCH₃ OCH₃ PO(CH₃)₂ CH₃ Het3 4256 OCH₂CH₃ OCH₂CH₃ PO(CH₃)₂ CH₃ Het3 4257 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₃)₂ CH₃ Het3 4258 SCH₃ SCH₃ PO(CH₃)₂ CH₃ Het3 4259 SCH₂CH₃ SCH₂CH₃ PO(CH₃)₂ CH₃ Het3 4260 N(CH₃)₂ N(CH₃)₂ PO(CH₃)₂ CH₃ Het3 4261 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₃)₂ CH₃ Het3 4262 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₃)₂ CH₃ Het3 4263 O—(CH₂CH₂)—O PO(CH₃)₂ CH₃ Het3 4264 O—(CH₂CH₂CH₂)—O PO(CH₃)₂ CH₃ Het3 4265 S—(CH₂CH₂)—S PO(CH₃)₂ CH₃ Het3 4266 S—(CH₂CH₂CH₂)—S PO(CH₃)₂ CH₃ Het3 4267 —(CH₂)₄— PO(CH₃)₂ CH₃ Het3 4268 —(CH₂)₅— PO(CH₃)₂ CH₃ Het3 4269 H H PO(CH₂CH₃)₂ CH₃ Het3 4270 CH₃ CH₃ PO(CH₂CH₃)₂ CH₃ Het3 4271 CH₂CH₃ CH₂CH₃ PO(CH₂CH₃)₂ CH₃ Het3 4272 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₂CH₃)₂ CH₃ Het3 4273 OCH₃ OCH₃ PO(CH₂CH₃)₂ CH₃ Het3 4274 OCH₂CH₃ OCH₂CH₃ PO(CH₂CH₃)₂ CH₃ Het3 4275 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₂CH₃)₂ CH₃ Het3 4276 SCH₃ SCH₃ PO(CH₂CH₃)₂ CH₃ Het3 4277 SCH₂CH₃ SCH₂CH₃ PO(CH₂CH₃)₂ CH₃ Het3 4278 N(CH₃)₂ N(CH₃)₂ PO(CH₂CH₃)₂ CH₃ Het3 4279 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₂CH₃)₂ CH₃ Het3 4280 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₂CH₃)₂ CH₃ Het3 4281 O—(CH₂CH₂)—O PO(CH₂CH₃)₂ CH₃ Het3 4282 O—(CH₂CH₂CH₂)—O PO(CH₂CH₃)₂ CH₃ Het3 4283 S—(CH₂CH₂)—S PO(CH₂CH₃)₂ CH₃ Het3 4284 S—(CH₂CH₂CH₂)—S PO(CH₂CH₃)₂ CH₃ Het3 4285 —(CH₂)₄— PO(CH₂CH₃)₂ CH₃ Het3 4286 —(CH₂)₅— PO(CH₂CH₃)₂ CH₃ Het3 4287 H H H Cl OH 4288 CH₃ CH₃ H Cl OH 4289 CH₂CH₃ CH₂CH₃ H Cl OH 4290 CH₂CH₂CH₃ CH₂CH₂CH₃ H Cl OH 4291 OCH₃ OCH₃ H Cl OH 4292 OCH₂CH₃ OCH₂CH₃ H Cl OH 4293 OCH₂CH₂CH₃ OCH₂CH₂CH₃ H Cl OH 4294 SCH₃ SCH₃ H Cl OH 4295 SCH₂CH₃ SCH₂CH₃ H Cl OH 4296 N(CH₃)₂ N(CH₃)₂ H Cl OH 4297 N(CH₂CH₃)₂ N(CH₂CH₃)₂ H Cl OH 4298 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) H Cl OH 4299 O—(CH₂CH₂)—O H Cl OH 4300 O—(CH₂CH₂CH₂)—O H Cl OH 4301 S—(CH₂CH₂)—S H Cl OH 4302 S—(CH₂CH₂CH₂)—S H Cl OH 4303 —(CH₂)₄— H Cl OH 4304 —(CH₂)₅— H Cl OH 4305 H H NO₂ Cl OH 4306 CH₃ CH₃ NO₂ Cl OH 4307 CH₂CH₃ CH₂CH₃ NO₂ Cl OH 4308 CH₂CH₂CH₃ CH₂CH₂CH₃ NO₂ Cl OH 4309 OCH₃ OCH₃ NO₂ Cl OH 4310 OCH₂CH₃ OCH₂CH₃ NO₂ Cl OH 4311 OCH₂CH₂CH₃ OCH₂CH₂CH₃ NO₂ Cl OH 4312 SCH₃ SCH₃ NO₂ Cl OH 4313 SCH₂CH₃ SCH₂CH₃ NO₂ Cl OH 4314 N(CH₃)₂ N(CH₃)₂ NO₂ Cl OH 4315 N(CH₂CH₃)₂ N(CH₂CH₃)₂ NO₂ Cl OH 4316 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) NO₂ Cl OH 4317 O—(CH₂CH₂)—O NO₂ Cl OH 4318 O—(CH₂CH₂CH₂)—O NO₂ Cl OH 4319 S—(CH₂CH₂)—S NO₂ Cl OH 4320 S—(CH₂CH₂CH₂)—S NO₂ Cl OH 4321 —(CH₂)₄— NO₂ Cl OH 4322 —(CH₂)₅— NO₂ Cl OH 4323 H H CN Cl OH 4324 CH₃ CH₃ CN Cl OH 4325 CH₂CH₃ CH₂CH₃ CN Cl OH 4326 CH₂CH₂CH₃ CH₂CH₂CH₃ CN Cl OH 4327 OCH₃ OCH₃ CN Cl OH 4328 OCH₂CH₃ OCH₂CH₃ CN Cl OH 4329 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CN Cl OH 4330 SCH₃ SCH₃ CN Cl OH 4331 SCH₂CH₃ SCH₂CH₃ CN Cl OH 4332 N(CH₃)₂ N(CH₃)₂ CN Cl OH 4333 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CN Cl OH 4334 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CN Cl OH 4335 O—(CH₂CH₂)—O CN Cl OH 4336 O—(CH₂CH₂CH₂)—O CN Cl OH 4337 S—(CH₂CH₂)—S CN Cl OH 4338 S—(CH₂CH₂CH₂)—S CN Cl OH 4339 —(CH₂)₄— CN Cl OH 4340 —(CH₂)₅— CN Cl OH 4341 H H F Cl OH 4342 CH₃ CH₃ F Cl OH 4343 CH₂CH₃ CH₂CH₃ F Cl OH 4344 CH₂CH₂CH₃ CH₂CH₂CH₃ F Cl OH 4345 OCH₃ OCH₃ F Cl OH 4346 OCH₂CH₃ OCH₂CH₃ F Cl OH 4347 OCH₂CH₂CH₃ OCH₂CH₂CH₃ F Cl OH 4348 SCH₃ SCH₃ F Cl OH 4349 SCH₂CH₃ SCH₂CH₃ F Cl OH 4350 N(CH₃)₂ N(CH₃)₂ F Cl OH 4351 N(CH₂CH₃)₂ N(CH₂CH₃)₂ F Cl OH 4352 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) F Cl OH 4353 O—(CH₂CH₂)—O F Cl OH 4354 O—(CH₂CH₂CH₂)—O F Cl OH 4355 S—(CH₂CH₂)—S F Cl OH 4356 S—(CH₂CH₂CH₂)—S F Cl OH 4357 —(CH₂)₄— F Cl OH 4358 —(CH₂)₅— F Cl OH 4359 H H Cl Cl OH 4360 CH₃ CH₃ Cl Cl OH 4361 CH₂CH₃ CH₂CH₃ Cl Cl OH 4362 CH₂CH₂CH₃ CH₂CH₂CH₃ Cl Cl OH 4363 OCH₃ OCH₃ Cl Cl OH 4364 OCH₂CH₃ OCH₂CH₃ Cl Cl OH 4365 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Cl Cl OH 4366 SCH₃ SCH₃ Cl Cl OH 4367 SCH₂CH₃ SCH₂CH₃ Cl Cl OH 4368 N(CH₃)₂ N(CH₃)₂ Cl Cl OH 4369 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Cl Cl OH 4370 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Cl Cl OH 4371 O—(CH₂CH₂)—O Cl Cl OH 4372 O—(CH₂CH₂CH₂)—O Cl Cl OH 4373 S—(CH₂CH₂)—S Cl Cl OH 4374 S—(CH₂CH₂CH₂)—S Cl Cl OH 4375 —(CH₂)₄— Cl Cl OH 4376 —(CH₂)₅— Cl Cl OH 4377 H H Br Cl OH 4378 CH₃ CH₃ Br Cl OH 4379 CH₂CH₃ CH₂CH₃ Br Cl OH 4380 CH₂CH₂CH₃ CH₂CH₂CH₃ Br Cl OH 4381 OCH₃ OCH₃ Br Cl OH 4382 OCH₂CH₃ OCH₂CH₃ Br Cl OH 4383 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Br Cl OH 4384 SCH₃ SCH₃ Br Cl OH 4385 SCH₂CH₃ SCH₂CH₃ Br Cl OH 4386 N(CH₃)₂ N(CH₃)₂ Br Cl OH 4387 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Br Cl OH 4388 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Br Cl OH 4389 O—(CH₂CH₂)—O Br Cl OH 4390 O—(CH₂CH₂CH₂)—O Br Cl OH 4391 S—(CH₂CH₂)—S Br Cl OH 4392 S—(CH₂CH₂CH₂)—S Br Cl OH 4393 —(CH₂)₄— Br Cl OH 4394 —(CH₂)₅— Br Cl OH 4395 H H CH₃ Cl OH 4396 CH₃ CH₃ CH₃ Cl OH 4397 CH₂CH₃ CH₂CH₃ CH₃ Cl OH 4398 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₃ Cl OH 4399 OCH₃ OCH₃ CH₃ Cl OH 4400 OCH₂CH₃ OCH₂CH₃ CH₃ Cl OH 4401 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₃ Cl OH 4402 SCH₃ SCH₃ CH₃ Cl OH 4403 SCH₂CH₃ SCH₂CH₃ CH₃ Cl OH 4404 N(CH₃)₂ N(CH₃)₂ CH₃ Cl OH 4405 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₃ Cl OH 4406 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₃ Cl OH 4407 O—(CH₂CH₂)—O CH₃ Cl OH 4408 O—(CH₂CH₂CH₂)—O CH₃ Cl OH 4409 S—(CH₂CH₂)—S CH₃ Cl OH 4410 S—(CH₂CH₂CH₂)—S CH₃ Cl OH 4411 —(CH₂)₄— CH₃ Cl OH 4412 —(CH₂)₅— CH₃ Cl OH 4413 H H CH₂CH₃ Cl OH 4414 CH₃ CH₃ CH₂CH₃ Cl OH 4415 CH₂CH₃ CH₂CH₃ CH₂CH₃ Cl OH 4416 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₂CH₃ Cl OH 4417 OCH₃ OCH₃ CH₂CH₃ Cl OH 4418 OCH₂CH₃ OCH₂CH₃ CH₂CH₃ Cl OH 4419 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₂CH₃ Cl OH 4420 SCH₃ SCH₃ CH₂CH₃ Cl OH 4421 SCH₂CH₃ SCH₂CH₃ CH₂CH₃ Cl OH 4422 N(CH₃)₂ N(CH₃)₂ CH₂CH₃ Cl OH 4423 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₂CH₃ Cl OH 4424 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₂CH₃ Cl OH 4425 O—(CH₂CH₂)—O CH₂CH₃ Cl OH 4426 O—(CH₂CH₂CH₂)—O CH₂CH₃ Cl OH 4427 S—(CH₂CH₂)—S CH₂CH₃ Cl OH 4428 S—(CH₂CH₂CH₂)—S CH₂CH₃ Cl OH 4429 —(CH₂)₄— CH₂CH₃ Cl OH 4430 —(CH₂)₅— CH₂CH₃ Cl OH 4431 H H CF₃ Cl OH 4432 CH₃ CH₃ CF₃ Cl OH 4433 CH₂CH₃ CH₂CH₃ CF₃ Cl OH 4434 CH₂CH₂CH₃ CH₂CH₂CH₃ CF₃ Cl OH 4435 OCH₃ OCH₃ CF₃ Cl OH 4436 OCH₂CH₃ OCH₂CH₃ CF₃ Cl OH 4437 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CF₃ Cl OH 4438 SCH₃ SCH₃ CF₃ Cl OH 4439 SCH₂CH₃ SCH₂CH₃ CF₃ Cl OH 4440 N(CH₃)₂ N(CH₃)₂ CF₃ Cl OH 4441 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CF₃ Cl OH 4442 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CF₃ Cl OH 4443 O—(CH₂CH₂)—O CF₃ Cl OH 4444 O—(CH₂CH₂CH₂)—O CF₃ Cl OH 4445 S—(CH₂CH₂)—S CF₃ Cl OH 4446 S—(CH₂CH₂CH₂)—S CF₃ Cl OH 4447 —(CH₂)₄— CF₃ Cl OH 4448 —(CH₂)₅— CF₃ Cl OH 4449 H H OCH₃ Cl OH 4450 CH₃ CH₃ OCH₃ Cl OH 4451 CH₂CH₃ CH₂CH₃ OCH₃ Cl OH 4452 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₃ Cl OH 4453 OCH₃ OCH₃ OCH₃ Cl OH 4454 OCH₂CH₃ OCH₂CH₃ OCH₃ Cl OH 4455 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₃ Cl OH 4456 SCH₃ SCH₃ OCH₃ Cl OH 4457 SCH₂CH₃ SCH₂CH₃ OCH₃ Cl OH 4458 N(CH₃)₂ N(CH₃)₂ OCH₃ Cl OH 4459 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₃ Cl OH 4460 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₃ Cl OH 4461 O—(CH₂CH₂)—O OCH₃ Cl OH 4462 O—(CH₂CH₂CH₂)—O OCH₃ Cl OH 4463 S—(CH₂CH₂)—S OCH₃ Cl OH 4464 S—(CH₂CH₂CH₂)—S OCH₃ Cl OH 4465 —(CH₂)₄— OCH₃ Cl OH 4466 —(CH₂)₅— OCH₃ Cl OH 4467 H H OCH₂CH₃ Cl OH 4468 CH₃ CH₃ OCH₂CH₃ Cl OH 4469 CH₂CH₃ CH₂CH₃ OCH₂CH₃ Cl OH 4470 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₂CH₃ Cl OH 4471 OCH₃ OCH₃ OCH₂CH₃ Cl OH 4472 OCH₂CH₃ OCH₂CH₃ OCH₂CH₃ Cl OH 4473 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₂CH₃ Cl OH 4474 SCH₃ SCH₃ OCH₂CH₃ Cl OH 4475 SCH₂CH₃ SCH₂CH₃ OCH₂CH₃ Cl OH 4476 N(CH₃)₂ N(CH₃)₂ OCH₂CH₃ Cl OH 4477 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₂CH₃ Cl OH 4478 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₂CH₃ Cl OH 4479 O—(CH₂CH₂)—O OCH₂CH₃ Cl OH 4480 O—(CH₂CH₂CH₂)—O OCH₂CH₃ Cl OH 4481 S—(CH₂CH₂)—S OCH₂CH₃ Cl OH 4482 S—(CH₂CH₂CH₂)—S OCH₂CH₃ Cl OH 4483 —(CH₂)₄— OCH₂CH₃ Cl OH 4484 —(CH₂)₅— OCH₂CH₃ Cl OH 4485 H H SCH₃ Cl OH 4486 CH₃ CH₃ SCH₃ Cl OH 4487 CH₂CH₃ CH₂CH₃ SCH₃ Cl OH 4488 CH₂CH₂CH₃ CH₂CH₂CH₃ SCH₃ Cl OH 4489 OCH₃ OCH₃ SCH₃ Cl OH 4490 OCH₂CH₃ OCH₂CH₃ SCH₃ Cl OH 4491 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SCH₃ Cl OH 4492 SCH₃ SCH₃ SCH₃ Cl OH 4493 SCH₂CH₃ SCH₂CH₃ SCH₃ Cl OH 4494 N(CH₃)₂ N(CH₃)₂ SCH₃ Cl OH 4495 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SCH₃ Cl OH 4496 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SCH₃ Cl OH 4497 O—(CH₂CH₂)—O SCH₃ Cl OH 4498 O—(CH₂CH₂CH₂)—O SCH₃ Cl OH 4499 S—(CH₂CH₂)—S SCH₃ Cl OH 4500 S—(CH₂CH₂CH₂)—S SCH₃ Cl OH 4501 —(CH₂)₄— SCH₃ Cl OH 4502 —(CH₂)₅— SCH₃ Cl OH 4503 H H SO₂CH₃ Cl OH 4504 CH₃ CH₃ SO₂CH₃ Cl OH 4505 CH₂CH₃ CH₂CH₃ SO₂CH₃ Cl OH 4506 CH₂CH₂CH₃ CH₂CH₂CH₃ SO₂CH₃ Cl OH 4507 OCH₃ OCH₃ SO₂CH₃ Cl OH 4508 OCH₂CH₃ OCH₂CH₃ SO₂CH₃ Cl OH 4509 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SO₂CH₃ Cl OH 4510 SCH₃ SCH₃ SO₂CH₃ Cl OH 4511 SCH₂CH₃ SCH₂CH₃ SO₂CH₃ Cl OH 4512 N(CH₃)₂ N(CH₃)₂ SO₂CH₃ Cl OH 4513 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SO₂CH₃ Cl OH 4514 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SO₂CH₃ Cl OH 4515 O—(CH₂CH₂)—O SO₂CH₃ Cl OH 4516 O—(CH₂CH₂CH₂)—O SO₂CH₃ Cl OH 4517 S—(CH₂CH₂)—S SO₂CH₃ Cl OH 4518 S—(CH₂CH₂CH₂)—S SO₂CH₃ Cl OH 4519 —(CH₂)₄— SO₂CH₃ Cl OH 4520 —(CH₂)₅— SO₂CH₃ Cl OH 4521 H H PO(OCH₃)₂ Cl OH 4522 CH₃ CH₃ PO(OCH₃)₂ Cl OH 4523 CH₂CH₃ CH₂CH₃ PO(OCH₃)₂ Cl OH 4524 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₃)₂ Cl OH 4525 OCH₃ OCH₃ PO(OCH₃)₂ Cl OH 4526 OCH₂CH₃ OCH₂CH₃ PO(OCH₃)₂ Cl OH 4527 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₃)₂ Cl OH 4528 SCH₃ SCH₃ PO(OCH₃)₂ Cl OH 4529 SCH₂CH₃ SCH₂CH₃ PO(OCH₃)₂ Cl OH 4530 N(CH₃)₂ N(CH₃)₂ PO(OCH₃)₂ Cl OH 4531 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₃)₂ Cl OH 4532 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₃)₂ Cl OH 4533 O—(CH₂CH₂)—O PO(OCH₃)₂ Cl OH 4534 O—(CH₂CH₂CH₂)—O PO(OCH₃)₂ Cl OH 4535 S—(CH₂CH₂)—S PO(OCH₃)₂ Cl OH 4536 S—(CH₂CH₂CH₂)—S PO(OCH₃)₂ Cl OH 4537 —(CH₂)₄— PO(OCH₃)₂ Cl OH 4538 —(CH₂)₅— PO(OCH₃)₂ Cl OH 4539 H H PO(OCH₂CH₃)₂ Cl OH 4540 CH₃ CH₃ PO(OCH₂CH₃)₂ Cl OH 4541 CH₂CH₃ CH₂CH₃ PO(OCH₂CH₃)₂ Cl OH 4542 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₂CH₃)₂ Cl OH 4543 OCH₃ OCH₃ PO(OCH₂CH₃)₂ Cl OH 4544 OCH₂CH₃ OCH₂CH₃ PO(OCH₂CH₃)₂ Cl OH 4545 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₂CH₃)₂ Cl OH 4546 SCH₃ SCH₃ PO(OCH₂CH₃)₂ Cl OH 4547 SCH₂CH₃ SCH₂CH₃ PO(OCH₂CH₃)₂ Cl OH 4548 N(CH₃)₂ N(CH₃)₂ PO(OCH₂CH₃)₂ Cl OH 4549 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₂CH₃)₂ Cl OH 4550 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₂CH₃)₂ Cl OH 4551 O—(CH₂CH₂)—O PO(OCH₂CH₃)₂ Cl OH 4552 O—(CH₂CH₂CH₂)—O PO(OCH₂CH₃)₂ Cl OH 4553 S—(CH₂CH₂)—S PO(OCH₂CH₃)₂ Cl OH 4554 S—(CH₂CH₂CH₂)—S PO(OCH₂CH₃)₂ Cl OH 4555 —(CH₂)₄— PO(OCH₂CH₃)₂ Cl OH 4556 —(CH₂)₅— PO(OCH₂CH₃)₂ Cl OH 4557 H H PO(CH₃)₂ Cl OH 4558 CH₃ CH₃ PO(CH₃)₂ Cl OH 4559 CH₂CH₃ CH₂CH₃ PO(CH₃)₂ Cl OH 4560 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₃)₂ Cl OH 4561 OCH₃ OCH₃ PO(CH₃)₂ Cl OH 4562 OCH₂CH₃ OCH₂CH₃ PO(CH₃)₂ Cl OH 4563 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₃)₂ Cl OH 4564 SCH₃ SCH₃ PO(CH₃)₂ Cl OH 4565 SCH₂CH₃ SCH₂CH₃ PO(CH₃)₂ Cl OH 4566 N(CH₃)₂ N(CH₃)₂ PO(CH₃)₂ Cl OH 4567 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₃)₂ Cl OH 4568 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₃)₂ Cl OH 4569 O—(CH₂CH₂)—O PO(CH₃)₂ Cl OH 4570 O—(CH₂CH₂CH₂)—O PO(CH₃)₂ Cl OH 4571 S—(CH₂CH₂)—S PO(CH₃)₂ Cl OH 4572 S—(CH₂CH₂CH₂)—S PO(CH₃)₂ Cl OH 4573 —(CH₂)₄— PO(CH₃)₂ Cl OH 4574 —(CH₂)₅— PO(CH₃)₂ Cl OH 4575 H H PO(CH₂CH₃)₂ Cl OH 4576 CH₃ CH₃ PO(CH₂CH₃)₂ Cl OH 4577 CH₂CH₃ CH₂CH₃ PO(CH₂CH₃)₂ Cl OH 4578 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₂CH₃)₂ Cl OH 4579 OCH₃ OCH₃ PO(CH₂CH₃)₂ Cl OH 4580 OCH₂CH₃ OCH₂CH₃ PO(CH₂CH₃)₂ Cl OH 4581 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₂CH₃)₂ Cl OH 4582 SCH₃ SCH₃ PO(CH₂CH₃)₂ Cl OH 4583 SCH₂CH₃ SCH₂CH₃ PO(CH₂CH₃)₂ Cl OH 4584 N(CH₃)₂ N(CH₃)₂ PO(CH₂CH₃)₂ Cl OH 4585 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₂CH₃)₂ Cl OH 4586 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₂CH₃)₂ Cl OH 4587 O—(CH₂CH₂)—O PO(CH₂CH₃)₂ Cl OH 4588 O—(CH₂CH₂CH₂)—O PO(CH₂CH₃)₂ Cl OH 4589 S—(CH₂CH₂)—S PO(CH₂CH₃)₂ Cl OH 4590 S—(CH₂CH₂CH₂)—S PO(CH₂CH₃)₂ Cl OH 4591 —(CH₂)₄— PO(CH₂CH₃)₂ Cl OH 4592 —(CH₂)₅— PO(CH₂CH₃)₂ Cl OH 4593 H H H Cl OCOC₆H₅ 4594 CH₃ CH₃ H Cl OCOC₆H₅ 4595 CH₂CH₃ CH₂CH₃ H Cl OCOC₆H₅ 4596 CH₂CH₂CH₃ CH₂CH₂CH₃ H Cl OCOC₆H₅ 4597 OCH₃ OCH₃ H Cl OCOC₆H₅ 4598 OCH₂CH₃ OCH₂CH₃ H Cl OCOC₆H₅ 4599 OCH₂CH₂CH₃ OCH₂CH₂CH₃ H Cl OCOC₆H₅ 4600 SCH₃ SCH₃ H Cl OCOC₆H₅ 4601 SCH₂CH₃ SCH₂CH₃ H Cl OCOC₆H₅ 4602 N(CH₃)₂ N(CH₃)₂ H Cl OCOC₆H₅ 4603 N(CH₂CH₃)₂ N(CH₂CH₃)₂ H Cl OCOC₆H₅ 4604 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) H Cl OCOC₆H₅ 4605 O—(CH₂CH₂)—O H Cl OCOC₆H₅ 4606 O—(CH₂CH₂CH₂)—O H Cl OCOC₆H₅ 4607 S—(CH₂CH₂)—S H Cl OCOC₆H₅ 4608 S—(CH₂CH₂CH₂)—S H Cl OCOC₆H₅ 4609 —(CH₂)₄— H Cl OCOC₆H₅ 4610 —(CH₂)₅— H Cl OCOC₆H₅ 4611 H H NO₂ Cl OCOC₆H₅ 4612 CH₃ CH₃ NO₂ Cl OCOC₆H₅ 4613 CH₂CH₃ CH₂CH₃ NO₂ Cl OCOC₆H₅ 4614 CH₂CH₂CH₃ CH₂CH₂CH₃ NO₂ Cl OCOC₆H₅ 4615 OCH₃ OCH₃ NO₂ Cl OCOC₆H₅ 4616 OCH₂CH₃ OCH₂CH₃ NO₂ Cl OCOC₆H₅ 4617 OCH₂CH₂CH₃ OCH₂CH₂CH₃ NO₂ Cl OCOC₆H₅ 4618 SCH₃ SCH₃ NO₂ Cl OCOC₆H₅ 4619 SCH₂CH₃ SCH₂CH₃ NO₂ Cl OCOC₆H₅ 4620 N(CH₃)₂ N(CH₃)₂ NO₂ Cl OCOC₆H₅ 4621 N(CH₂CH₃)₂ N(CH₂CH₃)₂ NO₂ Cl OCOC₆H₅ 4622 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) NO₂ Cl OCOC₆H₅ 4623 O—(CH₂CH₂)—O NO₂ Cl OCOC₆H₅ 4624 O—(CH₂CH₂CH₂)—O NO₂ Cl OCOC₆H₅ 4625 S—(CH₂CH₂)—S NO₂ Cl OCOC₆H₅ 4626 S—(CH₂CH₂CH₂)—S NO₂ Cl OCOC₆H₅ 4627 —(CH₂)₄— NO₂ Cl OCOC₆H₅ 4628 —(CH₂)₅— NO₂ Cl OCOC₆H₅ 4629 H H CN Cl OCOC₆H₅ 4630 CH₃ CH₃ CN Cl OCOC₆H₅ 4631 CH₂CH₃ CH₂CH₃ CN Cl OCOC₆H₅ 4632 CH₂CH₂CH₃ CH₂CH₂CH₃ CN Cl OCOC₆H₅ 4633 OCH₃ OCH₃ CN Cl OCOC₆H₅ 4634 OCH₂CH₃ OCH₂CH₃ CN Cl OCOC₆H₅ 4635 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CN Cl OCOC₆H₅ 4636 SCH₃ SCH₃ CN Cl OCOC₆H₅ 4637 SCH₂CH₃ SCH₂CH₃ CN Cl OCOC₆H₅ 4638 N(CH₃)₂ N(CH₃)₂ CN Cl OCOC₆H₅ 4639 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CN Cl OCOC₆H₅ 4640 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CN Cl OCOC₆H₅ 4641 O—(CH₂CH₂)—O CN Cl OCOC₆H₅ 4642 O—(CH₂CH₂CH₂)—O CN Cl OCOC₆H₅ 4643 S—(CH₂CH₂)—S CN Cl OCOC₆H₅ 4644 S—(CH₂CH₂CH₂)—S CN Cl OCOC₆H₅ 4645 —(CH₂)₄— CN Cl OCOC₆H₅ 4646 —(CH₂)₅— CN Cl OCOC₆H₅ 4647 H H F Cl OCOC₆H₅ 4648 CH₃ CH₃ F Cl OCOC₆H₅ 4649 CH₂CH₃ CH₂CH₃ F Cl OCOC₆H₅ 4650 CH₂CH₂CH₃ CH₂CH₂CH₃ F Cl OCOC₆H₅ 4651 OCH₃ OCH₃ F Cl OCOC₆H₅ 4652 OCH₂CH₃ OCH₂CH₃ F Cl OCOC₆H₅ 4653 OCH₂CH₂CH₃ OCH₂CH₂CH₃ F Cl OCOC₆H₅ 4654 SCH₃ SCH₃ F Cl OCOC₆H₅ 4655 SCH₂CH₃ SCH₂CH₃ F Cl OCOC₆H₅ 4656 N(CH₃)₂ N(CH₃)₂ F Cl OCOC₆H₅ 4657 N(CH₂CH₃)₂ N(CH₂CH₃)₂ F Cl OCOC₆H₅ 4658 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) F Cl OCOC₆H₅ 4659 O—(CH₂CH₂)—O F Cl OCOC₆H₅ 4660 O—(CH₂CH₂CH₂)—O F Cl OCOC₆H₅ 4661 S—(CH₂CH₂)—S F Cl OCOC₆H₅ 4662 S—(CH₂CH₂CH₂)—S F Cl OCOC₆H₅ 4663 —(CH₂)₄— F Cl OCOC₆H₅ 4664 —(CH₂)₅— F Cl OCOC₆H₅ 4665 H H Cl Cl OCOC₆H₅ 4666 CH₃ CH₃ Cl Cl OCOC₆H₅ 4667 CH₂CH₃ CH₂CH₃ Cl Cl OCOC₆H₅ 4668 CH₂CH₂CH₃ CH₂CH₂CH₃ Cl Cl OCOC₆H₅ 4669 OCH₃ OCH₃ Cl Cl OCOC₆H₅ 4670 OCH₂CH₃ OCH₂CH₃ Cl Cl OCOC₆H₅ 4671 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Cl Cl OCOC₆H₅ 4672 SCH₃ SCH₃ Cl Cl OCOC₆H₅ 4673 SCH₂CH₃ SCH₂CH₃ Cl Cl OCOC₆H₅ 4674 N(CH₃)₂ N(CH₃)₂ Cl Cl OCOC₆H₅ 4675 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Cl Cl OCOC₆H₅ 4676 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Cl Cl OCOC₆H₅ 4677 O—(CH₂CH₂)—O Cl Cl OCOC₆H₅ 4678 O—(CH₂CH₂CH₂)—O Cl Cl OCOC₆H₅ 4679 S—(CH₂CH₂)—S Cl Cl OCOC₆H₅ 4680 S—(CH₂CH₂CH₂)—S Cl Cl OCOC₆H₅ 4681 —(CH₂)₄— Cl Cl OCOC₆H₅ 4682 —(CH₂)₅— Cl Cl OCOC₆H₅ 4683 H H Br Cl OCOC₆H₅ 4684 CH₃ CH₃ Br Cl OCOC₆H₅ 4685 CH₂CH₃ CH₂CH₃ Br Cl OCOC₆H₅ 4686 CH₂CH₂CH₃ CH₂CH₂CH₃ Br Cl OCOC₆H₅ 4687 OCH₃ OCH₃ Br Cl OCOC₆H₅ 4688 OCH₂CH₃ OCH₂CH₃ Br Cl OCOC₆H₅ 4689 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Br Cl OCOC₆H₅ 4690 SCH₃ SCH₃ Br Cl OCOC₆H₅ 4691 SCH₂CH₃ SCH₂CH₃ Br Cl OCOC₆H₅ 4692 N(CH₃)₂ N(CH₃)₂ Br Cl OCOC₆H₅ 4693 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Br Cl OCOC₆H₅ 4694 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Br Cl OCOC₆H₅ 4695 O—(CH₂CH₂)—O Br Cl OCOC₆H₅ 4696 O—(CH₂CH₂CH₂)—O Br Cl OCOC₆H₅ 4697 S—(CH₂CH₂)—S Br Cl OCOC₆H₅ 4698 S—(CH₂CH₂CH₂)—S Br Cl OCOC₆H₅ 4699 —(CH₂)₄— Br Cl OCOC₆H₅ 4700 —(CH₂)₅— Br Cl OCOC₆H₅ 4701 H H CH₃ Cl OCOC₆H₅ 4702 CH₃ CH₃ CH₃ Cl OCOC₆H₅ 4703 CH₂CH₃ CH₂CH₃ CH₃ Cl OCOC₆H₅ 4704 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₃ Cl OCOC₆H₅ 4705 OCH₃ OCH₃ CH₃ Cl OCOC₆H₅ 4706 OCH₂CH₃ OCH₂CH₃ CH₃ Cl OCOC₆H₅ 4707 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₃ Cl OCOC₆H₅ 4708 SCH₃ SCH₃ CH₃ Cl OCOC₆H₅ 4709 SCH₂CH₃ SCH₂CH₃ CH₃ Cl OCOC₆H₅ 4710 N(CH₃)₂ N(CH₃)₂ CH₃ Cl OCOC₆H₅ 4711 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₃ Cl OCOC₆H₅ 4712 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₃ Cl OCOC₆H₅ 4713 O—(CH₂CH₂)—O CH₃ Cl OCOC₆H₅ 4714 O—(CH₂CH₂CH₂)—O CH₃ Cl OCOC₆H₅ 4715 S—(CH₂CH₂)—S CH₃ Cl OCOC₆H₅ 4716 S—(CH₂CH₂CH₂)—S CH₃ Cl OCOC₆H₅ 4717 —(CH₂)₄— CH₃ Cl OCOC₆H₅ 4718 —(CH₂)₅— CH₃ Cl OCOC₆H₅ 4719 H H CH₂CH₃ Cl OCOC₆H₅ 4720 CH₃ CH₃ CH₂CH₃ Cl OCOC₆H₅ 4721 CH₂CH₃ CH₂CH₃ CH₂CH₃ Cl OCOC₆H₅ 4722 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₂CH₃ Cl OCOC₆H₅ 4723 OCH₃ OCH₃ CH₂CH₃ Cl OCOC₆H₅ 4724 OCH₂CH₃ OCH₂CH₃ CH₂CH₃ Cl OCOC₆H₅ 4725 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₂CH₃ Cl OCOC₆H₅ 4726 SCH₃ SCH₃ CH₂CH₃ Cl OCOC₆H₅ 4727 SCH₂CH₃ SCH₂CH₃ CH₂CH₃ Cl OCOC₆H₅ 4728 N(CH₃)₂ N(CH₃)₂ CH₂CH₃ Cl OCOC₆H₅ 4729 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₂CH₃ Cl OCOC₆H₅ 4730 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₂CH₃ Cl OCOC₆H₅ 4731 O—(CH₂CH₂)—O CH₂CH₃ Cl OCOC₆H₅ 4732 O—(CH₂CH₂CH₂)—O CH₂CH₃ Cl OCOC₆H₅ 4733 S—(CH₂CH₂)—S CH₂CH₃ Cl OCOC₆H₅ 4734 S—(CH₂CH₂CH₂)—S CH₂CH₃ Cl OCOC₆H₅ 4735 —(CH₂)₄— CH₂CH₃ Cl OCOC₆H₅ 4736 —(CH₂)₅— CH₂CH₃ Cl OCOC₆H₅ 4737 H H CF₃ Cl OCOC₆H₅ 4738 CH₃ CH₃ CF₃ Cl OCOC₆H₅ 4739 CH₂CH₃ CH₂CH₃ CF₃ Cl OCOC₆H₅ 4740 CH₂CH₂CH₃ CH₂CH₂CH₃ CF₃ Cl OCOC₆H₅ 4741 OCH₃ OCH₃ CF₃ Cl OCOC₆H₅ 4742 OCH₂CH₃ OCH₂CH₃ CF₃ Cl OCOC₆H₅ 4743 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CF₃ Cl OCOC₆H₅ 4744 SCH₃ SCH₃ CF₃ Cl OCOC₆H₅ 4745 SCH₂CH₃ SCH₂CH₃ CF₃ Cl OCOC₆H₅ 4746 N(CH₃)₂ N(CH₃)₂ CF₃ Cl OCOC₆H₅ 4747 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CF₃ Cl OCOC₆H₅ 4748 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CF₃ Cl OCOC₆H₅ 4749 O—(CH₂CH₂)—O CF₃ Cl OCOC₆H₅ 4750 O—(CH₂CH₂CH₂)—O CF₃ Cl OCOC₆H₅ 4751 S—(CH₂CH₂)—S CF₃ Cl OCOC₆H₅ 4752 S—(CH₂CH₂CH₂)—S CF₃ Cl OCOC₆H₅ 4753 —(CH₂)₄— CF₃ Cl OCOC₆H₅ 4754 —(CH₂)₅— CF₃ Cl OCOC₆H₅ 4755 H H OCH₃ Cl OCOC₆H₅ 4756 CH₃ CH₃ OCH₃ Cl OCOC₆H₅ 4757 CH₂CH₃ CH₂CH₃ OCH₃ Cl OCOC₆H₅ 4758 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₃ Cl OCOC₆H₅ 4759 OCH₃ OCH₃ OCH₃ Cl OCOC₆H₅ 4760 OCH₂CH₃ OCH₂CH₃ OCH₃ Cl OCOC₆H₅ 4761 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₃ Cl OCOC₆H₅ 4762 SCH₃ SCH₃ OCH₃ Cl OCOC₆H₅ 4763 SCH₂CH₃ SCH₂CH₃ OCH₃ Cl OCOC₆H₅ 4764 N(CH₃)₂ N(CH₃)₂ OCH₃ Cl OCOC₆H₅ 4765 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₃ Cl OCOC₆H₅ 4766 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₃ Cl OCOC₆H₅ 4767 O—(CH₂CH₂)—O OCH₃ Cl OCOC₆H₅ 4768 O—(CH₂CH₂CH₂)—O OCH₃ Cl OCOC₆H₅ 4769 S—(CH₂CH₂)—S OCH₃ Cl OCOC₆H₅ 4770 S—(CH₂CH₂CH₂)—S OCH₃ Cl OCOC₆H₅ 4771 —(CH₂)₄— OCH₃ Cl OCOC₆H₅ 4772 —(CH₂)₅— OCH₃ Cl OCOC₆H₅ 4773 H H OCH₂CH₃ Cl OCOC₆H₅ 4774 CH₃ CH₃ OCH₂CH₃ Cl OCOC₆H₅ 4775 CH₂CH₃ CH₂CH₃ OCH₂CH₃ Cl OCOC₆H₅ 4776 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₂CH₃ Cl OCOC₆H₅ 4777 OCH₃ OCH₃ OCH₂CH₃ Cl OCOC₆H₅ 4778 OCH₂CH₃ OCH₂CH₃ OCH₂CH₃ Cl OCOC₆H₅ 4779 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₂CH₃ Cl OCOC₆H₅ 4780 SCH₃ SCH₃ OCH₂CH₃ Cl OCOC₆H₅ 4781 SCH₂CH₃ SCH₂CH₃ OCH₂CH₃ Cl OCOC₆H₅ 4782 N(CH₃)₂ N(CH₃)₂ OCH₂CH₃ Cl OCOC₆H₅ 4783 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₂CH₃ Cl OCOC₆H₅ 4784 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₂CH₃ Cl OCOC₆H₅ 4785 O—(CH₂CH₂)—O OCH₂CH₃ Cl OCOC₆H₅ 4786 O—(CH₂CH₂CH₂)—O OCH₂CH₃ Cl OCOC₆H₅ 4787 S—(CH₂CH₂)—S OCH₂CH₃ Cl OCOC₆H₅ 4788 S—(CH₂CH₂CH₂)—S OCH₂CH₃ Cl OCOC₆H₅ 4789 —(CH₂)₄— OCH₂CH₃ Cl OCOC₆H₅ 4790 —(CH₂)₅— OCH₂CH₃ Cl OCOC₆H₅ 4791 H H SCH₃ Cl OCOC₆H₅ 4792 CH₃ CH₃ SCH₃ Cl OCOC₆H₅ 4793 CH₂CH₃ CH₂CH₃ SCH₃ Cl OCOC₆H₅ 4794 CH₂CH₂CH₃ CH₂CH₂CH₃ SCH₃ Cl OCOC₆H₅ 4795 OCH₃ OCH₃ SCH₃ Cl OCOC₆H₅ 4796 OCH₂CH₃ OCH₂CH₃ SCH₃ Cl OCOC₆H₅ 4797 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SCH₃ Cl OCOC₆H₅ 4798 SCH₃ SCH₃ SCH₃ Cl OCOC₆H₅ 4799 SCH₂CH₃ SCH₂CH₃ SCH₃ Cl OCOC₆H₅ 4800 N(CH₃)₂ N(CH₃)₂ SCH₃ Cl OCOC₆H₅ 4801 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SCH₃ Cl OCOC₆H₅ 4802 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SCH₃ Cl OCOC₆H₅ 4803 O—(CH₂CH₂)—O SCH₃ Cl OCOC₆H₅ 4804 O—(CH₂CH₂CH₂)—O SCH₃ Cl OCOC₆H₅ 4805 S—(CH₂CH₂)—S SCH₃ Cl OCOC₆H₅ 4806 S—(CH₂CH₂CH₂)—S SCH₃ Cl OCOC₆H₅ 4807 —(CH₂)₄— SCH₃ Cl OCOC₆H₅ 4808 —(CH₂)₅— SCH₃ Cl OCOC₆H₅ 4809 H H SO₂CH₃ Cl OCOC₆H₅ 4810 CH₃ CH₃ SO₂CH₃ Cl OCOC₆H₅ 4811 CH₂CH₃ CH₂CH₃ SO₂CH₃ Cl OCOC₆H₅ 4812 CH₂CH₂CH₃ CH₂CH₂CH₃ SO₂CH₃ Cl OCOC₆H₅ 4813 OCH₃ OCH₃ SO₂CH₃ Cl OCOC₆H₅ 4814 OCH₂CH₃ OCH₂CH₃ SO₂CH₃ Cl OCOC₆H₅ 4815 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SO₂CH₃ Cl OCOC₆H₅ 4816 SCH₃ SCH₃ SO₂CH₃ Cl OCOC₆H₅ 4817 SCH₂CH₃ SCH₂CH₃ SO₂CH₃ Cl OCOC₆H₅ 4818 N(CH₃)₂ N(CH₃)₂ SO₂CH₃ Cl OCOC₆H₅ 4819 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SO₂CH₃ Cl OCOC₆H₅ 4820 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SO₂CH₃ Cl OCOC₆H₅ 4821 O—(CH₂CH₂)—O SO₂CH₃ Cl OCOC₆H₅ 4822 O—(CH₂CH₂CH₂)—O SO₂CH₃ Cl OCOC₆H₅ 4823 S—(CH₂CH₂)—S SO₂CH₃ Cl OCOC₆H₅ 4824 S—(CH₂CH₂CH₂)—S SO₂CH₃ Cl OCOC₆H₅ 4825 —(CH₂)₄— SO₂CH₃ Cl OCOC₆H₅ 4826 —(CH₂)₅— SO₂CH₃ Cl OCOC₆H₅ 4827 H H PO(OCH₃)₂ Cl OCOC₆H₅ 4828 CH₃ CH₃ PO(OCH₃)₂ Cl OCOC₆H₅ 4829 CH₂CH₃ CH₂CH₃ PO(OCH₃)₂ Cl OCOC₆H₅ 4830 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₃)₂ Cl OCOC₆H₅ 4831 OCH₃ OCH₃ PO(OCH₃)₂ Cl OCOC₆H₅ 4832 OCH₂CH₃ OCH₂CH₃ PO(OCH₃)₂ Cl OCOC₆H₅ 4833 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₃)₂ Cl OCOC₆H₅ 4834 SCH₃ SCH₃ PO(OCH₃)₂ Cl OCOC₆H₅ 4835 SCH₂CH₃ SCH₂CH₃ PO(OCH₃)₂ Cl OCOC₆H₅ 4836 N(CH₃)₂ N(CH₃)₂ PO(OCH₃)₂ Cl OCOC₆H₅ 4837 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₃)₂ Cl OCOC₆H₅ 4838 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₃)₂ Cl OCOC₆H₅ 4839 O—(CH₂CH₂)—O PO(OCH₃)₂ Cl OCOC₆H₅ 4840 O—(CH₂CH₂CH₂)—O PO(OCH₃)₂ Cl OCOC₆H₅ 4841 S—(CH₂CH₂)—S PO(OCH₃)₂ Cl OCOC₆H₅ 4842 S—(CH₂CH₂CH₂)—S PO(OCH₃)₂ Cl OCOC₆H₅ 4843 —(CH₂)₄— PO(OCH₃)₂ Cl OCOC₆H₅ 4844 —(CH₂)₅— PO(OCH₃)₂ Cl OCOC₆H₅ 4845 H H PO(OCH₂CH₃)₂ Cl OCOC₆H₅ 4846 CH₃ CH₃ PO(OCH₂CH₃)₂ Cl OCOC₆H₅ 4847 CH₂CH₃ CH₂CH₃ PO(OCH₂CH₃)₂ Cl OCOC₆H₅ 4848 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₂CH₃)₂ Cl OCOC₆H₅ 4849 OCH₃ OCH₃ PO(OCH₂CH₃)₂ Cl OCOC₆H₅ 4850 OCH₂CH₃ OCH₂CH₃ PO(OCH₂CH₃)₂ Cl OCOC₆H₅ 4851 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₂CH₃)₂ Cl OCOC₆H₅ 4852 SCH₃ SCH₃ PO(OCH₂CH₃)₂ Cl OCOC₆H₅ 4853 SCH₂CH₃ SCH₂CH₃ PO(OCH₂CH₃)₂ Cl OCOC₆H₅ 4854 N(CH₃)₂ N(CH₃)₂ PO(OCH₂CH₃)₂ Cl OCOC₆H₅ 4855 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₂CH₃)₂ Cl OCOC₆H₅ 4856 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₂CH₃)₂ Cl OCOC₆H₅ 4857 O—(CH₂CH₂)—O PO(OCH₂CH₃)₂ Cl OCOC₆H₅ 4858 O—(CH₂CH₂CH₂)—O PO(OCH₂CH₃)₂ Cl OCOC₆H₅ 4859 S—(CH₂CH₂)—S PO(OCH₂CH₃)₂ Cl OCOC₆H₅ 4860 S—(CH₂CH₂CH₂)—S PO(OCH₂CH₃)₂ Cl OCOC₆H₅ 4861 —(CH₂)₄— PO(OCH₂CH₃)₂ Cl OCOC₆H₅ 4862 —(CH₂)₅— PO(OCH₂CH₃)₂ Cl OCOC₆H₅ 4863 H H PO(CH₃)₂ Cl OCOC₆H₅ 4864 CH₃ CH₃ PO(CH₃)₂ Cl OCOC₆H₅ 4865 CH₂CH₃ CH₂CH₃ PO(CH₃)₂ Cl OCOC₆H₅ 4866 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₃)₂ Cl OCOC₆H₅ 4867 OCH₃ OCH₃ PO(CH₃)₂ Cl OCOC₆H₅ 4868 OCH₂CH₃ OCH₂CH₃ PO(CH₃)₂ Cl OCOC₆H₅ 4869 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₃)₂ Cl OCOC₆H₅ 4870 SCH₃ SCH₃ PO(CH₃)₂ Cl OCOC₆H₅ 4871 SCH₂CH₃ SCH₂CH₃ PO(CH₃)₂ Cl OCOC₆H₅ 4872 N(CH₃)₂ N(CH₃)₂ PO(CH₃)₂ Cl OCOC₆H₅ 4873 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₃)₂ Cl OCOC₆H₅ 4874 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₃)₂ Cl OCOC₆H₅ 4875 O—(CH₂CH₂)—O PO(CH₃)₂ Cl OCOC₆H₅ 4876 O—(CH₂CH₂CH₂)—O PO(CH₃)₂ Cl OCOC₆H₅ 4877 S—(CH₂CH₂)—S PO(CH₃)₂ Cl OCOC₆H₅ 4878 S—(CH₂CH₂CH₂)—S PO(CH₃)₂ Cl OCOC₆H₅ 4879 —(CH₂)₄— PO(CH₃)₂ Cl OCOC₆H₅ 4880 —(CH₂)₅— PO(CH₃)₂ Cl OCOC₆H₅ 4881 H H PO(CH₂CH₃)₂ Cl OCOC₆H₅ 4882 CH₃ CH₃ PO(CH₂CH₃)₂ Cl OCOC₆H₅ 4883 CH₂CH₃ CH₂CH₃ PO(CH₂CH₃)₂ Cl OCOC₆H₅ 4884 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₂CH₃)₂ Cl OCOC₆H₅ 4885 OCH₃ OCH₃ PO(CH₂CH₃)₂ Cl OCOC₆H₅ 4886 OCH₂CH₃ OCH₂CH₃ PO(CH₂CH₃)₂ Cl OCOC₆H₅ 4887 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₂CH₃)₂ Cl OCOC₆H₅ 4888 SCH₃ SCH₃ PO(CH₂CH₃)₂ Cl OCOC₆H₅ 4889 SCH₂CH₃ SCH₂CH₃ PO(CH₂CH₃)₂ Cl OCOC₆H₅ 4890 N(CH₃)₂ N(CH₃)₂ PO(CH₂CH₃)₂ Cl OCOC₆H₅ 4891 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₂CH₃)₂ Cl OCOC₆H₅ 4892 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₂CH₃)₂ Cl OCOC₆H₅ 4893 O—(CH₂CH₂)—O PO(CH₂CH₃)₂ Cl OCOC₆H₅ 4894 O—(CH₂CH₂CH₂)—O PO(CH₂CH₃)₂ Cl OCOC₆H₅ 4895 S—(CH₂CH₂)—S PO(CH₂CH₃)₂ Cl OCOC₆H₅ 4896 S—(CH₂CH₂CH₂)—S PO(CH₂CH₃)₂ Cl OCOC₆H₅ 4897 —(CH₂)₄— PO(CH₂CH₃)₂ Cl OCOC₆H₅ 4898 —(CH₂)₅— PO(CH₂CH₃)₂ Cl OCOC₆H₅ 4899 H H H Cl SCH₃ 4900 CH₃ CH₃ H Cl SCH₃ 4901 CH₂CH₃ CH₂CH₃ H Cl SCH₃ 4902 CH₂CH₂CH₃ CH₂CH₂CH₃ H Cl SCH₃ 4903 OCH₃ OCH₃ H Cl SCH₃ 4904 OCH₂CH₃ OCH₂CH₃ H Cl SCH₃ 4905 OCH₂CH₂CH₃ OCH₂CH₂CH₃ H Cl SCH₃ 4906 SCH₃ SCH₃ H Cl SCH₃ 4907 SCH₂CH₃ SCH₂CH₃ H Cl SCH₃ 4908 N(CH₃)₂ N(CH₃)₂ H Cl SCH₃ 4909 N(CH₂CH₃)₂ N(CH₂CH₃)₂ H Cl SCH₃ 4910 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) H Cl SCH₃ 4911 O—(CH₂CH₂)—O H Cl SCH₃ 4912 O—(CH₂CH₂CH₂)—O H Cl SCH₃ 4913 S—(CH₂CH₂)—S H Cl SCH₃ 4914 S—(CH₂CH₂CH₂)—S H Cl SCH₃ 4915 —(CH₂)₄— H Cl SCH₃ 4916 —(CH₂)₅— H Cl SCH₃ 4917 H H NO₂ Cl SCH₃ 4918 CH₃ CH₃ NO₂ Cl SCH₃ 4919 CH₂CH₃ CH₂CH₃ NO₂ Cl SCH₃ 4920 CH₂CH₂CH₃ CH₂CH₂CH₃ NO₂ Cl SCH₃ 4921 OCH₃ OCH₃ NO₂ Cl SCH₃ 4922 OCH₂CH₃ OCH₂CH₃ NO₂ Cl SCH₃ 4923 OCH₂CH₂CH₃ OCH₂CH₂CH₃ NO₂ Cl SCH₃ 4924 SCH₃ SCH₃ NO₂ Cl SCH₃ 4925 SCH₂CH₃ SCH₂CH₃ NO₂ Cl SCH₃ 4926 N(CH₃)₂ N(CH₃)₂ NO₂ Cl SCH₃ 4927 N(CH₂CH₃)₂ N(CH₂CH₃)₂ NO₂ Cl SCH₃ 4928 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) NO₂ Cl SCH₃ 4929 O—(CH₂CH₂)—O NO₂ Cl SCH₃ 4930 O—(CH₂CH₂CH₂)—O NO₂ Cl SCH₃ 4931 S—(CH₂CH₂)—S NO₂ Cl SCH₃ 4932 S—(CH₂CH₂CH₂)—S NO₂ Cl SCH₃ 4933 —(CH₂)₄— NO₂ Cl SCH₃ 4934 —(CH₂)₅— NO₂ Cl SCH₃ 4935 H H CN Cl SCH₃ 4936 CH₃ CH₃ CN Cl SCH₃ 4937 CH₂CH₃ CH₂CH₃ CN Cl SCH₃ 4938 CH₂CH₂CH₃ CH₂CH₂CH₃ CN Cl SCH₃ 4939 OCH₃ OCH₃ CN Cl SCH₃ 4940 OCH₂CH₃ OCH₂CH₃ CN Cl SCH₃ 4941 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CN Cl SCH₃ 4942 SCH₃ SCH₃ CN Cl SCH₃ 4943 SCH₂CH₃ SCH₂CH₃ CN Cl SCH₃ 4944 N(CH₃)₂ N(CH₃)₂ CN Cl SCH₃ 4945 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CN Cl SCH₃ 4946 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CN Cl SCH₃ 4947 O—(CH₂CH₂)—O CN Cl SCH₃ 4948 O—(CH₂CH₂CH₂)—O CN Cl SCH₃ 4949 S—(CH₂CH₂)—S CN Cl SCH₃ 4950 S—(CH₂CH₂CH₂)—S CN Cl SCH₃ 4951 —(CH₂)₄— CN Cl SCH₃ 4952 —(CH₂)₅— CN Cl SCH₃ 4953 H H F Cl SCH₃ 4954 CH₃ CH₃ F Cl SCH₃ 4955 CH₂CH₃ CH₂CH₃ F Cl SCH₃ 4956 CH₂CH₂CH₃ CH₂CH₂CH₃ F Cl SCH₃ 4957 OCH₃ OCH₃ F Cl SCH₃ 4958 OCH₂CH₃ OCH₂CH₃ F Cl SCH₃ 4959 OCH₂CH₂CH₃ OCH₂CH₂CH₃ F Cl SCH₃ 4960 SCH₃ SCH₃ F Cl SCH₃ 4961 SCH₂CH₃ SCH₂CH₃ F Cl SCH₃ 4962 N(CH₃)₂ N(CH₃)₂ F Cl SCH₃ 4963 N(CH₂CH₃)₂ N(CH₂CH₃)₂ F Cl SCH₃ 4964 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) F Cl SCH₃ 4965 O—(CH₂CH₂)—O F Cl SCH₃ 4966 O—(CH₂CH₂CH₂)—O F Cl SCH₃ 4967 S—(CH₂CH₂)—S F Cl SCH₃ 4968 S—(CH₂CH₂CH₂)—S F Cl SCH₃ 4969 —(CH₂)₄— F Cl SCH₃ 4970 —(CH₂)₅— F Cl SCH₃ 4971 H H Cl Cl SCH₃ 4972 CH₃ CH₃ Cl Cl SCH₃ 4973 CH₂CH₃ CH₂CH₃ Cl Cl SCH₃ 4974 CH₂CH₂CH₃ CH₂CH₂CH₃ Cl Cl SCH₃ 4975 OCH₃ OCH₃ Cl Cl SCH₃ 4976 OCH₂CH₃ OCH₂CH₃ Cl Cl SCH₃ 4977 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Cl Cl SCH₃ 4978 SCH₃ SCH₃ Cl Cl SCH₃ 4979 SCH₂CH₃ SCH₂CH₃ Cl Cl SCH₃ 4980 N(CH₃)₂ N(CH₃)₂ Cl Cl SCH₃ 4981 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Cl Cl SCH₃ 4982 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Cl Cl SCH₃ 4983 O—(CH₂CH₂)—O Cl Cl SCH₃ 4984 O—(CH₂CH₂CH₂)—O Cl Cl SCH₃ 4985 S—(CH₂CH₂)—S Cl Cl SCH₃ 4986 S—(CH₂CH₂CH₂)—S Cl Cl SCH₃ 4987 —(CH₂)₄— Cl Cl SCH₃ 4988 —(CH₂)₅— Cl Cl SCH₃ 4989 H H Br Cl SCH₃ 4990 CH₃ CH₃ Br Cl SCH₃ 4991 CH₂CH₃ CH₂CH₃ Br Cl SCH₃ 4992 CH₂CH₂CH₃ CH₂CH₂CH₃ Br Cl SCH₃ 4993 OCH₃ OCH₃ Br Cl SCH₃ 4994 OCH₂CH₃ OCH₂CH₃ Br Cl SCH₃ 4995 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Br Cl SCH₃ 4996 SCH₃ SCH₃ Br Cl SCH₃ 4997 SCH₂CH₃ SCH₂CH₃ Br Cl SCH₃ 4998 N(CH₃)₂ N(CH₃)₂ Br Cl SCH₃ 4999 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Br Cl SCH₃ 5000 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Br Cl SCH₃ 5001 O—(CH₂CH₂)—O Br Cl SCH₃ 5002 O—(CH₂CH₂CH₂)—O Br Cl SCH₃ 5003 S—(CH₂CH₂)—S Br Cl SCH₃ 5004 S—(CH₂CH₂CH₂)—S Br Cl SCH₃ 5005 —(CH₂)₄— Br Cl SCH₃ 5006 —(CH₂)₅— Br Cl SCH₃ 5007 H H CH₃ Cl SCH₃ 5008 CH₃ CH₃ CH₃ Cl SCH₃ 5009 CH₂CH₃ CH₂CH₃ CH₃ Cl SCH₃ 5010 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₃ Cl SCH₃ 5011 OCH₃ OCH₃ CH₃ Cl SCH₃ 5012 OCH₂CH₃ OCH₂CH₃ CH₃ Cl SCH₃ 5013 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₃ Cl SCH₃ 5014 SCH₃ SCH₃ CH₃ Cl SCH₃ 5015 SCH₂CH₃ SCH₂CH₃ CH₃ Cl SCH₃ 5016 N(CH₃)₂ N(CH₃)₂ CH₃ Cl SCH₃ 5017 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₃ Cl SCH₃ 5018 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₃ Cl SCH₃ 5019 O—(CH₂CH₂)—O CH₃ Cl SCH₃ 5020 O—(CH₂CH₂CH₂)—O CH₃ Cl SCH₃ 5021 S—(CH₂CH₂)—S CH₃ Cl SCH₃ 5022 S—(CH₂CH₂CH₂)—S CH₃ Cl SCH₃ 5023 —(CH₂)₄— CH₃ Cl SCH₃ 5024 —(CH₂)₅— CH₃ Cl SCH₃ 5025 H H CH₂CH₃ Cl SCH₃ 5026 CH₃ CH₃ CH₂CH₃ Cl SCH₃ 5027 CH₂CH₃ CH₂CH₃ CH₂CH₃ Cl SCH₃ 5028 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₂CH₃ Cl SCH₃ 5029 OCH₃ OCH₃ CH₂CH₃ Cl SCH₃ 5030 OCH₂CH₃ OCH₂CH₃ CH₂CH₃ Cl SCH₃ 5031 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₂CH₃ Cl SCH₃ 5032 SCH₃ SCH₃ CH₂CH₃ Cl SCH₃ 5033 SCH₂CH₃ SCH₂CH₃ CH₂CH₃ Cl SCH₃ 5034 N(CH₃)₂ N(CH₃)₂ CH₂CH₃ Cl SCH₃ 5035 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₂CH₃ Cl SCH₃ 5036 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₂CH₃ Cl SCH₃ 5037 O—(CH₂CH₂)—O CH₂CH₃ Cl SCH₃ 5038 O—(CH₂CH₂CH₂)—O CH₂CH₃ Cl SCH₃ 5039 S—(CH₂CH₂)—S CH₂CH₃ Cl SCH₃ 5040 S—(CH₂CH₂CH₂)—S CH₂CH₃ Cl SCH₃ 5041 —(CH₂)₄— CH₂CH₃ Cl SCH₃ 5042 —(CH₂)₅— CH₂CH₃ Cl SCH₃ 5043 H H CF₃ Cl SCH₃ 5044 CH₃ CH₃ CF₃ Cl SCH₃ 5045 CH₂CH₃ CH₂CH₃ CF₃ Cl SCH₃ 5046 CH₂CH₂CH₃ CH₂CH₂CH₃ CF₃ Cl SCH₃ 5047 OCH₃ OCH₃ CF₃ Cl SCH₃ 5048 OCH₂CH₃ OCH₂CH₃ CF₃ Cl SCH₃ 5049 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CF₃ Cl SCH₃ 5050 SCH₃ SCH₃ CF₃ Cl SCH₃ 5051 SCH₂CH₃ SCH₂CH₃ CF₃ Cl SCH₃ 5052 N(CH₃)₂ N(CH₃)₂ CF₃ Cl SCH₃ 5053 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CF₃ Cl SCH₃ 5054 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CF₃ Cl SCH₃ 5055 O—(CH₂CH₂)—O CF₃ Cl SCH₃ 5056 O—(CH₂CH₂CH₂)—O CF₃ Cl SCH₃ 5057 S—(CH₂CH₂)—S CF₃ Cl SCH₃ 5058 S—(CH₂CH₂CH₂)—S CF₃ Cl SCH₃ 5059 —(CH₂)₄— CF₃ Cl SCH₃ 5060 —(CH₂)₅— CF₃ Cl SCH₃ 5061 H H OCH₃ Cl SCH₃ 5062 CH₃ CH₃ OCH₃ Cl SCH₃ 5063 CH₂CH₃ CH₂CH₃ OCH₃ Cl SCH₃ 5064 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₃ Cl SCH₃ 5065 OCH₃ OCH₃ OCH₃ Cl SCH₃ 5066 OCH₂CH₃ OCH₂CH₃ OCH₃ Cl SCH₃ 5067 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₃ Cl SCH₃ 5068 SCH₃ SCH₃ OCH₃ Cl SCH₃ 5069 SCH₂CH₃ SCH₂CH₃ OCH₃ Cl SCH₃ 5070 N(CH₃)₂ N(CH₃)₂ OCH₃ Cl SCH₃ 5071 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₃ Cl SCH₃ 5072 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₃ Cl SCH₃ 5073 O—(CH₂CH₂)—O OCH₃ Cl SCH₃ 5074 O—(CH₂CH₂CH₂)—O OCH₃ Cl SCH₃ 5075 S—(CH₂CH₂)—S OCH₃ Cl SCH₃ 5076 S—(CH₂CH₂CH₂)—S OCH₃ Cl SCH₃ 5077 —(CH₂)₄— OCH₃ Cl SCH₃ 5078 —(CH₂)₅— OCH₃ Cl SCH₃ 5079 H H OCH₂CH₃ Cl SCH₃ 5080 CH₃ CH₃ OCH₂CH₃ Cl SCH₃ 5081 CH₂CH₃ CH₂CH₃ OCH₂CH₃ Cl SCH₃ 5082 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₂CH₃ Cl SCH₃ 5083 OCH₃ OCH₃ OCH₂CH₃ Cl SCH₃ 5084 OCH₂CH₃ OCH₂CH₃ OCH₂CH₃ Cl SCH₃ 5085 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₂CH₃ Cl SCH₃ 5086 SCH₃ SCH₃ OCH₂CH₃ Cl SCH₃ 5087 SCH₂CH₃ SCH₂CH₃ OCH₂CH₃ Cl SCH₃ 5088 N(CH₃)₂ N(CH₃)₂ OCH₂CH₃ Cl SCH₃ 5089 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₂CH₃ Cl SCH₃ 5090 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₂CH₃ Cl SCH₃ 5091 O—(CH₂CH₂)—O OCH₂CH₃ Cl SCH₃ 5092 O—(CH₂CH₂CH₂)—O OCH₂CH₃ Cl SCH₃ 5093 S—(CH₂CH₂)—S OCH₂CH₃ Cl SCH₃ 5094 S—(CH₂CH₂CH₂)—S OCH₂CH₃ Cl SCH₃ 5095 —(CH₂)₄— OCH₂CH₃ Cl SCH₃ 5096 —(CH₂)₅— OCH₂CH₃ Cl SCH₃ 5097 H H SCH₃ Cl SCH₃ 5098 CH₃ CH₃ SCH₃ Cl SCH₃ 5099 CH₂CH₃ CH₂CH₃ SCH₃ Cl SCH₃ 5100 CH₂CH₂CH₃ CH₂CH₂CH₃ SCH₃ Cl SCH₃ 5101 OCH₃ OCH₃ SCH₃ Cl SCH₃ 5102 OCH₂CH₃ OCH₂CH₃ SCH₃ Cl SCH₃ 5103 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SCH₃ Cl SCH₃ 5104 SCH₃ SCH₃ SCH₃ Cl SCH₃ 5105 SCH₂CH₃ SCH₂CH₃ SCH₃ Cl SCH₃ 5106 N(CH₃)₂ N(CH₃)₂ SCH₃ Cl SCH₃ 5107 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SCH₃ Cl SCH₃ 5108 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SCH₃ Cl SCH₃ 5109 O—(CH₂CH₂)—O SCH₃ Cl SCH₃ 5110 O—(CH₂CH₂CH₂)—O SCH₃ Cl SCH₃ 5111 S—(CH₂CH₂)—S SCH₃ Cl SCH₃ 5112 S—(CH₂CH₂CH₂)—S SCH₃ Cl SCH₃ 5113 —(CH₂)₄— SCH₃ Cl SCH₃ 5114 —(CH₂)₅— SCH₃ Cl SCH₃ 5115 H H SO₂CH₃ Cl SCH₃ 5116 CH₃ CH₃ SO₂CH₃ Cl SCH₃ 5117 CH₂CH₃ CH₂CH₃ SO₂CH₃ Cl SCH₃ 5118 CH₂CH₂CH₃ CH₂CH₂CH₃ SO₂CH₃ Cl SCH₃ 5119 OCH₃ OCH₃ SO₂CH₃ Cl SCH₃ 5120 OCH₂CH₃ OCH₂CH₃ SO₂CH₃ Cl SCH₃ 5121 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SO₂CH₃ Cl SCH₃ 5122 SCH₃ SCH₃ SO₂CH₃ Cl SCH₃ 5123 SCH₂CH₃ SCH₂CH₃ SO₂CH₃ Cl SCH₃ 5124 N(CH₃)₂ N(CH₃)₂ SO₂CH₃ Cl SCH₃ 5125 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SO₂CH₃ Cl SCH₃ 5126 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SO₂CH₃ Cl SCH₃ 5127 O—(CH₂CH₂)—O SO₂CH₃ Cl SCH₃ 5128 O—(CH₂CH₂CH₂)—O SO₂CH₃ Cl SCH₃ 5129 S—(CH₂CH₂)—S SO₂CH₃ Cl SCH₃ 5130 S—(CH₂CH₂CH₂)—S SO₂CH₃ Cl SCH₃ 5131 —(CH₂)₄— SO₂CH₃ Cl SCH₃ 5132 —(CH₂)₅— SO₂CH₃ Cl SCH₃ 5133 H H PO(OCH₃)₂ Cl SCH₃ 5134 CH₃ CH₃ PO(OCH₃)₂ Cl SCH₃ 5135 CH₂CH₃ CH₂CH₃ PO(OCH₃)₂ Cl SCH₃ 5136 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₃)₂ Cl SCH₃ 5137 OCH₃ OCH₃ PO(OCH₃)₂ Cl SCH₃ 5138 OCH₂CH₃ OCH₂CH₃ PO(OCH₃)₂ Cl SCH₃ 5139 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₃)₂ Cl SCH₃ 5140 SCH₃ SCH₃ PO(OCH₃)₂ Cl SCH₃ 5141 SCH₂CH₃ SCH₂CH₃ PO(OCH₃)₂ Cl SCH₃ 5142 N(CH₃)₂ N(CH₃)₂ PO(OCH₃)₂ Cl SCH₃ 5143 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₃)₂ Cl SCH₃ 5144 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₃)₂ Cl SCH₃ 5145 O—(CH₂CH₂)—O PO(OCH₃)₂ Cl SCH₃ 5146 O—(CH₂CH₂CH₂)—O PO(OCH₃)₂ Cl SCH₃ 5147 S—(CH₂CH₂)—S PO(OCH₃)₂ Cl SCH₃ 5148 S—(CH₂CH₂CH₂)—S PO(OCH₃)₂ Cl SCH₃ 5149 —(CH₂)₄— PO(OCH₃)₂ Cl SCH₃ 5150 —(CH₂)₅— PO(OCH₃)₂ Cl SCH₃ 5151 H H PO(OCH₂CH₃)₂ Cl SCH₃ 5152 CH₃ CH₃ PO(OCH₂CH₃)₂ Cl SCH₃ 5153 CH₂CH₃ CH₂CH₃ PO(OCH₂CH₃)₂ Cl SCH₃ 5154 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₂CH₃)₂ Cl SCH₃ 5155 OCH₃ OCH₃ PO(OCH₂CH₃)₂ Cl SCH₃ 5156 OCH₂CH₃ OCH₂CH₃ PO(OCH₂CH₃)₂ Cl SCH₃ 5157 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₂CH₃)₂ Cl SCH₃ 5158 SCH₃ SCH₃ PO(OCH₂CH₃)₂ Cl SCH₃ 5159 SCH₂CH₃ SCH₂CH₃ PO(OCH₂CH₃)₂ Cl SCH₃ 5160 N(CH₃)₂ N(CH₃)₂ PO(OCH₂CH₃)₂ Cl SCH₃ 5161 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₂CH₃)₂ Cl SCH₃ 5162 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₂CH₃)₂ Cl SCH₃ 5163 O—(CH₂CH₂)—O PO(OCH₂CH₃)₂ Cl SCH₃ 5164 O—(CH₂CH₂CH₂)—O PO(OCH₂CH₃)₂ Cl SCH₃ 5165 S—(CH₂CH₂)—S PO(OCH₂CH₃)₂ Cl SCH₃ 5166 S—(CH₂CH₂CH₂)—S PO(OCH₂CH₃)₂ Cl SCH₃ 5167 —(CH₂)₄— PO(OCH₂CH₃)₂ Cl SCH₃ 5168 —(CH₂)₅— PO(OCH₂CH₃)₂ Cl SCH₃ 5169 H H PO(CH₃)₂ Cl SCH₃ 5170 CH₃ CH₃ PO(CH₃)₂ Cl SCH₃ 5171 CH₂CH₃ CH₂CH₃ PO(CH₃)₂ Cl SCH₃ 5172 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₃)₂ Cl SCH₃ 5173 OCH₃ OCH₃ PO(CH₃)₂ Cl SCH₃ 5174 OCH₂CH₃ OCH₂CH₃ PO(CH₃)₂ Cl SCH₃ 5175 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₃)₂ Cl SCH₃ 5176 SCH₃ SCH₃ PO(CH₃)₂ Cl SCH₃ 5177 SCH₂CH₃ SCH₂CH₃ PO(CH₃)₂ Cl SCH₃ 5178 N(CH₃)₂ N(CH₃)₂ PO(CH₃)₂ Cl SCH₃ 5179 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₃)₂ Cl SCH₃ 5180 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₃)₂ Cl SCH₃ 5181 O—(CH₂CH₂)—O PO(CH₃)₂ Cl SCH₃ 5182 O—(CH₂CH₂CH₂)—O PO(CH₃)₂ Cl SCH₃ 5183 S—(CH₂CH₂)—S PO(CH₃)₂ Cl SCH₃ 5184 S—(CH₂CH₂CH₂)—S PO(CH₃)₂ Cl SCH₃ 5185 —(CH₂)₄— PO(CH₃)₂ Cl SCH₃ 5186 —(CH₂)₅— PO(CH₃)₂ Cl SCH₃ 5187 H H PO(CH₂CH₃)₂ Cl SCH₃ 5188 CH₃ CH₃ PO(CH₂CH₃)₂ Cl SCH₃ 5189 CH₂CH₃ CH₂CH₃ PO(CH₂CH₃)₂ Cl SCH₃ 5190 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₂CH₃)₂ Cl SCH₃ 5191 OCH₃ OCH₃ PO(CH₂CH₃)₂ Cl SCH₃ 5192 OCH₂CH₃ OCH₂CH₃ PO(CH₂CH₃)₂ Cl SCH₃ 5193 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₂CH₃)₂ Cl SCH₃ 5194 SCH₃ SCH₃ PO(CH₂CH₃)₂ Cl SCH₃ 5195 SCH₂CH₃ SCH₂CH₃ PO(CH₂CH₃)₂ Cl SCH₃ 5196 N(CH₃)₂ N(CH₃)₂ PO(CH₂CH₃)₂ Cl SCH₃ 5197 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₂CH₃)₂ Cl SCH₃ 5198 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₂CH₃)₂ Cl SCH₃ 5199 O—(CH₂CH₂)—O PO(CH₂CH₃)₂ Cl SCH₃ 5200 O—(CH₂CH₂CH₂)—O PO(CH₂CH₃)₂ Cl SCH₃ 5201 S—(CH₂CH₂)—S PO(CH₂CH₃)₂ Cl SCH₃ 5202 S—(CH₂CH₂CH₂)—S PO(CH₂CH₃)₂ Cl SCH₃ 5203 —(CH₂)₄— PO(CH₂CH₃)₂ Cl SCH₃ 5204 —(CH₂)₅— PO(CH₂CH₃)₂ Cl SCH₃ 5205 H H H Cl SC₆H₅ 5206 CH₃ CH₃ H Cl SC₆H₅ 5207 CH₂CH₃ CH₂CH₃ H Cl SC₆H₅ 5208 CH₂CH₂CH₃ CH₂CH₂CH₃ H Cl SC₆H₅ 5209 OCH₃ OCH₃ H Cl SC₆H₅ 5210 OCH₂CH₃ OCH₂CH₃ H Cl SC₆H₅ 5211 OCH₂CH₂CH₃ OCH₂CH₂CH₃ H Cl SC₆H₅ 5212 SCH₃ SCH₃ H Cl SC₆H₅ 5213 SCH₂CH₃ SCH₂CH₃ H Cl SC₆H₅ 5214 N(CH₃)₂ N(CH₃)₂ H Cl SC₆H₅ 5215 N(CH₂CH₃)₂ N(CH₂CH₃)₂ H Cl SC₆H₅ 5216 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) H Cl SC₆H₅ 5217 O—(CH₂CH₂)—O H Cl SC₆H₅ 5218 O—(CH₂CH₂CH₂)—O H Cl SC₆H₅ 5219 S—(CH₂CH₂)—S H Cl SC₆H₅ 5220 S—(CH₂CH₂CH₂)—S H Cl SC₆H₅ 5221 —(CH₂)₄— H Cl SC₆H₅ 5222 —(CH₂)₅— H Cl SC₆H₅ 5223 H H NO₂ Cl SC₆H₅ 5224 CH₃ CH₃ NO₂ Cl SC₆H₅ 5225 CH₂CH₃ CH₂CH₃ NO₂ Cl SC₆H₅ 5226 CH₂CH₂CH₃ CH₂CH₂CH₃ NO₂ Cl SC₆H₅ 5227 OCH₃ OCH₃ NO₂ Cl SC₆H₅ 5228 OCH₂CH₃ OCH₂CH₃ NO₂ Cl SC₆H₅ 5229 OCH₂CH₂CH₃ OCH₂CH₂CH₃ NO₂ Cl SC₆H₅ 5230 SCH₃ SCH₃ NO₂ Cl SC₆H₅ 5231 SCH₂CH₃ SCH₂CH₃ NO₂ Cl SC₆H₅ 5232 N(CH₃)₂ N(CH₃)₂ NO₂ Cl SC₆H₅ 5233 N(CH₂CH₃)₂ N(CH₂CH₃)₂ NO₂ Cl SC₆H₅ 5234 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) NO₂ Cl SC₆H₅ 5235 O—(CH₂CH₂)—O NO₂ Cl SC₆H₅ 5236 O—(CH₂CH₂CH₂)—O NO₂ Cl SC₆H₅ 5237 S—(CH₂CH₂)—S NO₂ Cl SC₆H₅ 5238 S—(CH₂CH₂CH₂)—S NO₂ Cl SC₆H₅ 5239 —(CH₂)₄— NO₂ Cl SC₆H₅ 5240 —(CH₂)₅— NO₂ Cl SC₆H₅ 5241 H H CN Cl SC₆H₅ 5242 CH₃ CH₃ CN Cl SC₆H₅ 5243 CH₂CH₃ CH₂CH₃ CN Cl SC₆H₅ 5244 CH₂CH₂CH₃ CH₂CH₂CH₃ CN Cl SC₆H₅ 5245 OCH₃ OCH₃ CN Cl SC₆H₅ 5246 OCH₂CH₃ OCH₂CH₃ CN Cl SC₆H₅ 5247 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CN Cl SC₆H₅ 5248 SCH₃ SCH₃ CN Cl SC₆H₅ 5249 SCH₂CH₃ SCH₂CH₃ CN Cl SC₆H₅ 5250 N(CH₃)₂ N(CH₃)₂ CN Cl SC₆H₅ 5251 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CN Cl SC₆H₅ 5252 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CN Cl SC₆H₅ 5253 O—(CH₂CH₂)—O CN Cl SC₆H₅ 5254 O—(CH₂CH₂CH₂)—O CN Cl SC₆H₅ 5255 S—(CH₂CH₂)—S CN Cl SC₆H₅ 5256 S—(CH₂CH₂CH₂)—S CN Cl SC₆H₅ 5257 —(CH₂)₄— CN Cl SC₆H₅ 5258 —(CH₂)₅— CN Cl SC₆H₅ 5259 H H F Cl SC₆H₅ 5260 CH₃ CH₃ F Cl SC₆H₅ 5261 CH₂CH₃ CH₂CH₃ F Cl SC₆H₅ 5262 CH₂CH₂CH₃ CH₂CH₂CH₃ F Cl SC₆H₅ 5263 OCH₃ OCH₃ F Cl SC₆H₅ 5264 OCH₂CH₃ OCH₂CH₃ F Cl SC₆H₅ 5265 OCH₂CH₂CH₃ OCH₂CH₂CH₃ F Cl SC₆H₅ 5266 SCH₃ SCH₃ F Cl SC₆H₅ 5267 SCH₂CH₃ SCH₂CH₃ F Cl SC₆H₅ 5268 N(CH₃)₂ N(CH₃)₂ F Cl SC₆H₅ 5269 N(CH₂CH₃)₂ N(CH₂CH₃)₂ F Cl SC₆H₅ 5270 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) F Cl SC₆H₅ 5271 O—(CH₂CH₂)—O F Cl SC₆H₅ 5272 O—(CH₂CH₂CH₂)—O F Cl SC₆H₅ 5273 S—(CH₂CH₂)—S F Cl SC₆H₅ 5274 S—(CH₂CH₂CH₂)—S F Cl SC₆H₅ 5275 —(CH₂)₄— F Cl SC₆H₅ 5276 —(CH₂)₅— F Cl SC₆H₅ 5277 H H Cl Cl SC₆H₅ 5278 CH₃ CH₃ Cl Cl SC₆H₅ 5279 CH₂CH₃ CH₂CH₃ Cl Cl SC₆H₅ 5280 CH₂CH₂CH₃ CH₂CH₂CH₃ Cl Cl SC₆H₅ 5281 OCH₃ OCH₃ Cl Cl SC₆H₅ 5282 OCH₂CH₃ OCH₂CH₃ Cl Cl SC₆H₅ 5283 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Cl Cl SC₆H₅ 5284 SCH₃ SCH₃ Cl Cl SC₆H₅ 5285 SCH₂CH₃ SCH₂CH₃ Cl Cl SC₆H₅ 5286 N(CH₃)₂ N(CH₃)₂ Cl Cl SC₆H₅ 5287 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Cl Cl SC₆H₅ 5288 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Cl Cl SC₆H₅ 5289 O—(CH₂CH₂)—O Cl Cl SC₆H₅ 5290 O—(CH₂CH₂CH₂)—O Cl Cl SC₆H₅ 5291 S—(CH₂CH₂)—S Cl Cl SC₆H₅ 5292 S—(CH₂CH₂CH₂)—S Cl Cl SC₆H₅ 5293 —(CH₂)₄— Cl Cl SC₆H₅ 5294 —(CH₂)₅— Cl Cl SC₆H₅ 5295 H H Br Cl SC₆H₅ 5296 CH₃ CH₃ Br Cl SC₆H₅ 5297 CH₂CH₃ CH₂CH₃ Br Cl SC₆H₅ 5298 CH₂CH₂CH₃ CH₂CH₂CH₃ Br Cl SC₆H₅ 5299 OCH₃ OCH₃ Br Cl SC₆H₅ 5300 OCH₂CH₃ OCH₂CH₃ Br Cl SC₆H₅ 5301 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Br Cl SC₆H₅ 5302 SCH₃ SCH₃ Br Cl SC₆H₅ 5303 SCH₂CH₃ SCH₂CH₃ Br Cl SC₆H₅ 5304 N(CH₃)₂ N(CH₃)₂ Br Cl SC₆H₅ 5305 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Br Cl SC₆H₅ 5306 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Br Cl SC₆H₅ 5307 O—(CH₂CH₂)—O Br Cl SC₆H₅ 5308 O—(CH₂CH₂CH₂)—O Br Cl SC₆H₅ 5309 S—(CH₂CH₂)—S Br Cl SC₆H₅ 5310 S—(CH₂CH₂CH₂)—S Br Cl SC₆H₅ 5311 —(CH₂)₄— Br Cl SC₆H₅ 5312 —(CH₂)₅— Br Cl SC₆H₅ 5313 H H CH₃ Cl SC₆H₅ 5314 CH₃ CH₃ CH₃ Cl SC₆H₅ 5315 CH₂CH₃ CH₂CH₃ CH₃ Cl SC₆H₅ 5316 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₃ Cl SC₆H₅ 5317 OCH₃ OCH₃ CH₃ Cl SC₆H₅ 5318 OCH₂CH₃ OCH₂CH₃ CH₃ Cl SC₆H₅ 5319 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₃ Cl SC₆H₅ 5320 SCH₃ SCH₃ CH₃ Cl SC₆H₅ 5321 SCH₂CH₃ SCH₂CH₃ CH₃ Cl SC₆H₅ 5322 N(CH₃)₂ N(CH₃)₂ CH₃ Cl SC₆H₅ 5323 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₃ Cl SC₆H₅ 5324 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₃ Cl SC₆H₅ 5325 O—(CH₂CH₂)—O CH₃ Cl SC₆H₅ 5326 O—(CH₂CH₂CH₂)—O CH₃ Cl SC₆H₅ 5327 S—(CH₂CH₂)—S CH₃ Cl SC₆H₅ 5328 S—(CH₂CH₂CH₂)—S CH₃ Cl SC₆H₅ 5329 —(CH₂)₄— CH₃ Cl SC₆H₅ 5330 —(CH₂)₅— CH₃ Cl SC₆H₅ 5331 H H CH₂CH₃ Cl SC₆H₅ 5332 CH₃ CH₃ CH₂CH₃ Cl SC₆H₅ 5333 CH₂CH₃ CH₂CH₃ CH₂CH₃ Cl SC₆H₅ 5334 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₂CH₃ Cl SC₆H₅ 5335 OCH₃ OCH₃ CH₂CH₃ Cl SC₆H₅ 5336 OCH₂CH₃ OCH₂CH₃ CH₂CH₃ Cl SC₆H₅ 5337 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₂CH₃ Cl SC₆H₅ 5338 SCH₃ SCH₃ CH₂CH₃ Cl SC₆H₅ 5339 SCH₂CH₃ SCH₂CH₃ CH₂CH₃ Cl SC₆H₅ 5340 N(CH₃)₂ N(CH₃)₂ CH₂CH₃ Cl SC₆H₅ 5341 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₂CH₃ Cl SC₆H₅ 5342 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₂CH₃ Cl SC₆H₅ 5343 O—(CH₂CH₂)—O CH₂CH₃ Cl SC₆H₅ 5344 O—(CH₂CH₂CH₂)—O CH₂CH₃ Cl SC₆H₅ 5345 S—(CH₂CH₂)—S CH₂CH₃ Cl SC₆H₅ 5346 S—(CH₂CH₂CH₂)—S CH₂CH₃ Cl SC₆H₅ 5347 —(CH₂)₄— CH₂CH₃ Cl SC₆H₅ 5348 —(CH₂)₅— CH₂CH₃ Cl SC₆H₅ 5349 H H CF₃ Cl SC₆H₅ 5350 CH₃ CH₃ CF₃ Cl SC₆H₅ 5351 CH₂CH₃ CH₂CH₃ CF₃ Cl SC₆H₅ 5352 CH₂CH₂CH₃ CH₂CH₂CH₃ CF₃ Cl SC₆H₅ 5353 OCH₃ OCH₃ CF₃ Cl SC₆H₅ 5354 OCH₂CH₃ OCH₂CH₃ CF₃ Cl SC₆H₅ 5355 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CF₃ Cl SC₆H₅ 5356 SCH₃ SCH₃ CF₃ Cl SC₆H₅ 5357 SCH₂CH₃ SCH₂CH₃ CF₃ Cl SC₆H₅ 5358 N(CH₃)₂ N(CH₃)₂ CF₃ Cl SC₆H₅ 5359 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CF₃ Cl SC₆H₅ 5360 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CF₃ Cl SC₆H₅ 5361 O—(CH₂CH₂)—O CF₃ Cl SC₆H₅ 5362 O—(CH₂CH₂CH₂)—O CF₃ Cl SC₆H₅ 5363 S—(CH₂CH₂)—S CF₃ Cl SC₆H₅ 5364 S—(CH₂CH₂CH₂)—S CF₃ Cl SC₆H₅ 5365 —(CH₂)₄— CF₃ Cl SC₆H₅ 5366 —(CH₂)₅— CF₃ Cl SC₆H₅ 5367 H H OCH₃ Cl SC₆H₅ 5368 CH₃ CH₃ OCH₃ Cl SC₆H₅ 5369 CH₂CH₃ CH₂CH₃ OCH₃ Cl SC₆H₅ 5370 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₃ Cl SC₆H₅ 5371 OCH₃ OCH₃ OCH₃ Cl SC₆H₅ 5372 OCH₂CH₃ OCH₂CH₃ OCH₃ Cl SC₆H₅ 5373 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₃ Cl SC₆H₅ 5374 SCH₃ SCH₃ OCH₃ Cl SC₆H₅ 5375 SCH₂CH₃ SCH₂CH₃ OCH₃ Cl SC₆H₅ 5376 N(CH₃)₂ N(CH₃)₂ OCH₃ Cl SC₆H₅ 5377 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₃ Cl SC₆H₅ 5378 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₃ Cl SC₆H₅ 5379 O—(CH₂CH₂)—O OCH₃ Cl SC₆H₅ 5380 O—(CH₂CH₂CH₂)—O OCH₃ Cl SC₆H₅ 5381 S—(CH₂CH₂)—S OCH₃ Cl SC₆H₅ 5382 S—(CH₂CH₂CH₂)—S OCH₃ Cl SC₆H₅ 5383 —(CH₂)₄— OCH₃ Cl SC₆H₅ 5384 —(CH₂)₅— OCH₃ Cl SC₆H₅ 5385 H H OCH₂CH₃ Cl SC₆H₅ 5386 CH₃ CH₃ OCH₂CH₃ Cl SC₆H₅ 5387 CH₂CH₃ CH₂CH₃ OCH₂CH₃ Cl SC₆H₅ 5388 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₂CH₃ Cl SC₆H₅ 5389 OCH₃ OCH₃ OCH₂CH₃ Cl SC₆H₅ 5390 OCH₂CH₃ OCH₂CH₃ OCH₂CH₃ Cl SC₆H₅ 5391 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₂CH₃ Cl SC₆H₅ 5392 SCH₃ SCH₃ OCH₂CH₃ Cl SC₆H₅ 5393 SCH₂CH₃ SCH₂CH₃ OCH₂CH₃ Cl SC₆H₅ 5394 N(CH₃)₂ N(CH₃)₂ OCH₂CH₃ Cl SC₆H₅ 5395 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₂CH₃ Cl SC₆H₅ 5396 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₂CH₃ Cl SC₆H₅ 5397 O—(CH₂CH₂)—O OCH₂CH₃ Cl SC₆H₅ 5398 O—(CH₂CH₂CH₂)—O OCH₂CH₃ Cl SC₆H₅ 5399 S—(CH₂CH₂)—S OCH₂CH₃ Cl SC₆H₅ 5400 S—(CH₂CH₂CH₂)—S OCH₂CH₃ Cl SC₆H₅ 5401 —(CH₂)₄— OCH₂CH₃ Cl SC₆H₅ 5402 —(CH₂)₅— OCH₂CH₃ Cl SC₆H₅ 5403 H H SCH₃ Cl SC₆H₅ 5404 CH₃ CH₃ SCH₃ Cl SC₆H₅ 5405 CH₂CH₃ CH₂CH₃ SCH₃ Cl SC₆H₅ 5406 CH₂CH₂CH₃ CH₂CH₂CH₃ SCH₃ Cl SC₆H₅ 5407 OCH₃ OCH₃ SCH₃ Cl SC₆H₅ 5408 OCH₂CH₃ OCH₂CH₃ SCH₃ Cl SC₆H₅ 5409 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SCH₃ Cl SC₆H₅ 5410 SCH₃ SCH₃ SCH₃ Cl SC₆H₅ 5411 SCH₂CH₃ SCH₂CH₃ SCH₃ Cl SC₆H₅ 5412 N(CH₃)₂ N(CH₃)₂ SCH₃ Cl SC₆H₅ 5413 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SCH₃ Cl SC₆H₅ 5414 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SCH₃ Cl SC₆H₅ 5415 O—(CH₂CH₂)—O SCH₃ Cl SC₆H₅ 5416 O—(CH₂CH₂CH₂)—O SCH₃ Cl SC₆H₅ 5417 S—(CH₂CH₂)—S SCH₃ Cl SC₆H₅ 5418 S—(CH₂CH₂CH₂)—S SCH₃ Cl SC₆H₅ 5419 —(CH₂)₄— SCH₃ Cl SC₆H₅ 5420 —(CH₂)₅— SCH₃ Cl SC₆H₅ 5421 H H SO₂CH₃ Cl SC₆H₅ 5422 CH₃ CH₃ SO₂CH₃ Cl SC₆H₅ 5423 CH₂CH₃ CH₂CH₃ SO₂CH₃ Cl SC₆H₅ 5424 CH₂CH₂CH₃ CH₂CH₂CH₃ SO₂CH₃ Cl SC₆H₅ 5425 OCH₃ OCH₃ SO₂CH₃ Cl SC₆H₅ 5426 OCH₂CH₃ OCH₂CH₃ SO₂CH₃ Cl SC₆H₅ 5427 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SO₂CH₃ Cl SC₆H₅ 5428 SCH₃ SCH₃ SO₂CH₃ Cl SC₆H₅ 5429 SCH₂CH₃ SCH₂CH₃ SO₂CH₃ Cl SC₆H₅ 5430 N(CH₃)₂ N(CH₃)₂ SO₂CH₃ Cl SC₆H₅ 5431 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SO₂CH₃ Cl SC₆H₅ 5432 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SO₂CH₃ Cl SC₆H₅ 5433 O—(CH₂CH₂)—O SO₂CH₃ Cl SC₆H₅ 5434 O—(CH₂CH₂CH₂)—O SO₂CH₃ Cl SC₆H₅ 5435 S—(CH₂CH₂)—S SO₂CH₃ Cl SC₆H₅ 5436 S—(CH₂CH₂CH₂)—S SO₂CH₃ Cl SC₆H₅ 5437 —(CH₂)₄— SO₂CH₃ Cl SC₆H₅ 5438 —(CH₂)₅— SO₂CH₃ Cl SC₆H₅ 5439 H H PO(OCH₃)₂ Cl SC₆H₅ 5440 CH₃ CH₃ PO(OCH₃)₂ Cl SC₆H₅ 5441 CH₂CH₃ CH₂CH₃ PO(OCH₃)₂ Cl SC₆H₅ 5442 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₃)₂ Cl SC₆H₅ 5443 OCH₃ OCH₃ PO(OCH₃)₂ Cl SC₆H₅ 5444 OCH₂CH₃ OCH₂CH₃ PO(OCH₃)₂ Cl SC₆H₅ 5445 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₃)₂ Cl SC₆H₅ 5446 SCH₃ SCH₃ PO(OCH₃)₂ Cl SC₆H₅ 5447 SCH₂CH₃ SCH₂CH₃ PO(OCH₃)₂ Cl SC₆H₅ 5448 N(CH₃)₂ N(CH₃)₂ PO(OCH₃)₂ Cl SC₆H₅ 5449 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₃)₂ Cl SC₆H₅ 5450 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₃)₂ Cl SC₆H₅ 5451 O—(CH₂CH₂)—O PO(OCH₃)₂ Cl SC₆H₅ 5452 O—(CH₂CH₂CH₂)—O PO(OCH₃)₂ Cl SC₆H₅ 5453 S—(CH₂CH₂)—S PO(OCH₃)₂ Cl SC₆H₅ 5454 S—(CH₂CH₂CH₂)—S PO(OCH₃)₂ Cl SC₆H₅ 5455 —(CH₂)₄— PO(OCH₃)₂ Cl SC₆H₅ 5456 —(CH₂)₅— PO(OCH₃)₂ Cl SC₆H₅ 5457 H H PO(OCH₂CH₃)₂ Cl SC₆H₅ 5458 CH₃ CH₃ PO(OCH₂CH₃)₂ Cl SC₆H₅ 5459 CH₂CH₃ CH₂CH₃ PO(OCH₂CH₃)₂ Cl SC₆H₅ 5460 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₂CH₃)₂ Cl SC₆H₅ 5461 OCH₃ OCH₃ PO(OCH₂CH₃)₂ Cl SC₆H₅ 5462 OCH₂CH₃ OCH₂CH₃ PO(OCH₂CH₃)₂ Cl SC₆H₅ 5463 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₂CH₃)₂ Cl SC₆H₅ 5464 SCH₃ SCH₃ PO(OCH₂CH₃)₂ Cl SC₆H₅ 5465 SCH₂CH₃ SCH₂CH₃ PO(OCH₂CH₃)₂ Cl SC₆H₅ 5466 N(CH₃)₂ N(CH₃)₂ PO(OCH₂CH₃)₂ Cl SC₆H₅ 5467 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₂CH₃)₂ Cl SC₆H₅ 5468 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₂CH₃)₂ Cl SC₆H₅ 5469 O—(CH₂CH₂)—O PO(OCH₂CH₃)₂ Cl SC₆H₅ 5470 O—(CH₂CH₂CH₂)—O PO(OCH₂CH₃)₂ Cl SC₆H₅ 5471 S—(CH₂CH₂)—S PO(OCH₂CH₃)₂ Cl SC₆H₅ 5472 S—(CH₂CH₂CH₂)—S PO(OCH₂CH₃)₂ Cl SC₆H₅ 5473 —(CH₂)₄— PO(OCH₂CH₃)₂ Cl SC₆H₅ 5474 —(CH₂)₅— PO(OCH₂CH₃)₂ Cl SC₆H₅ 5475 H H PO(CH₃)₂ Cl SC₆H₅ 5476 CH₃ CH₃ PO(CH₃)₂ Cl SC₆H₅ 5477 CH₂CH₃ CH₂CH₃ PO(CH₃)₂ Cl SC₆H₅ 5478 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₃)₂ Cl SC₆H₅ 5479 OCH₃ OCH₃ PO(CH₃)₂ Cl SC₆H₅ 5480 OCH₂CH₃ OCH₂CH₃ PO(CH₃)₂ Cl SC₆H₅ 5481 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₃)₂ Cl SC₆H₅ 5482 SCH₃ SCH₃ PO(CH₃)₂ Cl SC₆H₅ 5483 SCH₂CH₃ SCH₂CH₃ PO(CH₃)₂ Cl SC₆H₅ 5484 N(CH₃)₂ N(CH₃)₂ PO(CH₃)₂ Cl SC₆H₅ 5485 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₃)₂ Cl SC₆H₅ 5486 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₃)₂ Cl SC₆H₅ 5487 O—(CH₂CH₂)—O PO(CH₃)₂ Cl SC₆H₅ 5488 O—(CH₂CH₂CH₂)—O PO(CH₃)₂ Cl SC₆H₅ 5489 S—(CH₂CH₂)—S PO(CH₃)₂ Cl SC₆H₅ 5490 S—(CH₂CH₂CH₂)—S PO(CH₃)₂ Cl SC₆H₅ 5491 —(CH₂)₄— PO(CH₃)₂ Cl SC₆H₅ 5492 —(CH₂)₅— PO(CH₃)₂ Cl SC₆H₅ 5493 H H PC(CH₂CH₃)₂ Cl SC₆H₅ 5494 CH₃ CH₃ PC(CH₂CH₃)₂ Cl SC₆H₅ 5495 CH₂CH₃ CH₂CH₃ PC(CH₂CH₃)₂ Cl SC₆H₅ 5496 CH₂CH₂CH₃ CH₂CH₂CH₃ PC(CH₂CH₃)₂ Cl SC₆H₅ 5497 OCH₃ OCH₃ PC(CH₂CH₃)₂ Cl SC₆H₅ 5498 OCH₂CH₃ OCH₂CH₃ PC(CH₂CH₃)₂ Cl SC₆H₅ 5499 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PC(CH₂CH₃)₂ Cl SC₆H₅ 5500 SCH₃ SCH₃ PC(CH₂CH₃)₂ Cl SC₆H₅ 5501 SCH₂CH₃ SCH₂CH₃ PC(CH₂CH₃)₂ Cl SC₆H₅ 5502 N(CH₃)₂ N(CH₃)₂ PC(CH₂CH₃)₂ Cl SC₆H₅ 5503 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PC(CH₂CH₃)₂ Cl SC₆H₅ 5504 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PC(CH₂CH₃)₂ Cl SC₆H₅ 5505 O—(CH₂CH₂)—O PC(CH₂CH₃)₂ Cl SC₆H₅ 5506 O—(CH₂CH₂CH₂)—O PC(CH₂CH₃)₂ Cl SC₆H₅ 5507 S—(CH₂CH₂)—S PC(CH₂CH₃)₂ Cl SC₆H₅ 5508 S—(CH₂CH₂CH₂)—S PC(CH₂CH₃)₂ Cl SC₆H₅ 5509 —(CH₂)₄— PC(CH₂CH₃)₂ Cl SC₆H₅ 5510 —(CH₂)₅— PC(CH₂CH₃)₂ Cl SC₆H₅ 5511 H H H Cl Het1 5512 CH₃ CH₃ H Cl Het1 5513 CH₂CH₃ CH₂CH₃ H Cl Het1 5514 CH₂CH₂CH₃ CH₂CH₂CH₃ H Cl Het1 5515 OCH₃ OCH₃ H Cl Het1 5516 OCH₂CH₃ OCH₂CH₃ H Cl Het1 5517 OCH₂CH₂CH₃ OCH₂CH₂CH₃ H Cl Het1 5518 SCH₃ SCH₃ H Cl Het1 5519 SCH₂CH₃ SCH₂CH₃ H Cl Het1 5520 N(CH₃)₂ N(CH₃)₂ H Cl Het1 5521 N(CH₂CH₃)₂ N(CH₂CH₃)₂ H Cl Het1 5522 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) H Cl Het1 5523 O—(CH₂CH₂)—O H Cl Het1 5524 O—(CH₂CH₂CH₂)—O H Cl Het1 5525 S—(CH₂CH₂)—S H Cl Het1 5526 S—(CH₂CH₂CH₂)—S H Cl Het1 5527 —(CH₂)₄— H Cl Het1 5528 —(CH₂)₅— H Cl Het1 5529 H H NO₂ Cl Het1 5530 CH₃ CH₃ NO₂ Cl Het1 5531 CH₂CH₃ CH₂CH₃ NO₂ Cl Het1 5532 CH₂CH₂CH₃ CH₂CH₂CH₃ NO₂ Cl Het1 5533 OCH₃ OCH₃ NO₂ Cl Het1 5534 OCH₂CH₃ OCH₂CH₃ NO₂ Cl Het1 5535 OCH₂CH₂CH₃ OCH₂CH₂CH₃ NO₂ Cl Het1 5536 SCH₃ SCH₃ NO₂ Cl Het1 5537 SCH₂CH₃ SCH₂CH₃ NO₂ Cl Het1 5538 N(CH₃)₂ N(CH₃)₂ NO₂ Cl Het1 5539 N(CH₂CH₃)₂ N(CH₂CH₃)₂ NO₂ Cl Het1 5540 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) NO₂ Cl Het1 5541 O—(CH₂CH₂)—O NO₂ Cl Het1 5542 O—(CH₂CH₂CH₂)—O NO₂ Cl Het1 5543 S—(CH₂CH₂)—S NO₂ Cl Het1 5544 S—(CH₂CH₂CH₂)—S NO₂ Cl Het1 5545 —(CH₂)₄— NO₂ Cl Het1 5546 —(CH₂)₅— NO₂ Cl Het1 5547 H H CN Cl Het1 5548 CH₃ CH₃ CN Cl Het1 5549 CH₂CH₃ CH₂CH₃ CN Cl Het1 5550 CH₂CH₂CH₃ CH₂CH₂CH₃ CN Cl Het1 5551 OCH₃ OCH₃ CN Cl Het1 5552 OCH₂CH₃ OCH₂CH₃ CN Cl Het1 5553 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CN Cl Het1 5554 SCH₃ SCH₃ CN Cl Het1 5555 SCH₂CH₃ SCH₂CH₃ CN Cl Het1 5556 N(CH₃)₂ N(CH₃)₂ CN Cl Het1 5557 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CN Cl Het1 5558 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CN Cl Het1 5559 O—(CH₂CH₂)—O CN Cl Het1 5560 O—(CH₂CH₂CH₂)—O CN Cl Het1 5561 S—(CH₂CH₂)—S CN Cl Het1 5562 S—(CH₂CH₂CH₂)—S CN Cl Het1 5563 —(CH₂)₄— CN Cl Het1 5564 —(CH₂)₅— CN Cl Het1 5565 H H F Cl Het1 5566 CH₃ CH₃ F Cl Het1 5567 CH₂CH₃ CH₂CH₃ F Cl Het1 5568 CH₂CH₂CH₃ CH₂CH₂CH₃ F Cl Het1 5569 OCH₃ OCH₃ F Cl Het1 5570 OCH₂CH₃ OCH₂CH₃ F Cl Het1 5571 OCH₂CH₂CH₃ OCH₂CH₂CH₃ F Cl Het1 5572 SCH₃ SCH₃ F Cl Het1 5573 SCH₂CH₃ SCH₂CH₃ F Cl Het1 5574 N(CH₃)₂ N(CH₃)₂ F Cl Het1 5575 N(CH₂CH₃)₂ N(CH₂CH₃)₂ F Cl Het1 5576 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) F Cl Het1 5577 O—(CH₂CH₂)—O F Cl Het1 5578 O—(CH₂CH₂CH₂)—O F Cl Het1 5579 S—(CH₂CH₂)—S F Cl Het1 5580 S—(CH₂CH₂CH₂)—S F Cl Het1 5581 —(CH₂)₄— F Cl Het1 5582 —(CH₂)₅— F Cl Het1 5583 H H Cl Cl Het1 5584 CH₃ CH₃ Cl Cl Het1 5585 CH₂CH₃ CH₂CH₃ Cl Cl Het1 5586 CH₂CH₂CH₃ CH₂CH₂CH₃ Cl Cl Het1 5587 OCH₃ OCH₃ Cl Cl Het1 5588 OCH₂CH₃ OCH₂CH₃ Cl Cl Het1 5589 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Cl Cl Het1 5590 SCH₃ SCH₃ Cl Cl Het1 5591 SCH₂CH₃ SCH₂CH₃ Cl Cl Het1 5592 N(CH₃)₂ N(CH₃)₂ Cl Cl Het1 5593 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Cl Cl Het1 5594 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Cl Cl Het1 5595 O—(CH₂CH₂)—O Cl Cl Het1 5596 O—(CH₂CH₂CH₂)—O Cl Cl Het1 5597 S—(CH₂CH₂)—S Cl Cl Het1 5598 S—(CH₂CH₂CH₂)—S Cl Cl Het1 5599 —(CH₂)₄— Cl Cl Het1 5600 —(CH₂)₅— Cl Cl Het1 5601 H H Br Cl Het1 5602 CH₃ CH₃ Br Cl Het1 5603 CH₂CH₃ CH₂CH₃ Br Cl Het1 5604 CH₂CH₂CH₃ CH₂CH₂CH₃ Br Cl Het1 5605 OCH₃ OCH₃ Br Cl Het1 5606 OCH₂CH₃ OCH₂CH₃ Br Cl Het1 5607 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Br Cl Het1 5608 SCH₃ SCH₃ Br Cl Het1 5609 SCH₂CH₃ SCH₂CH₃ Br Cl Het1 5610 N(CH₃)₂ N(CH₃)₂ Br Cl Het1 5611 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Br Cl Het1 5612 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Br Cl Het1 5613 O—(CH₂CH₂)—O Br Cl Het1 5614 O—(CH₂CH₂CH₂)—O Br Cl Het1 5615 S—(CH₂CH₂)—S Br Cl Het1 5616 S—(CH₂CH₂CH₂)—S Br Cl Het1 5617 —(CH₂)₄— Br Cl Het1 5618 —(CH₂)₅— Br Cl Het1 5619 H H CH₃ Cl Het1 5620 CH₃ CH₃ CH₃ Cl Het1 5621 CH₂CH₃ CH₂CH₃ CH₃ Cl Het1 5622 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₃ Cl Het1 5623 OCH₃ OCH₃ CH₃ Cl Het1 5624 OCH₂CH₃ OCH₂CH₃ CH₃ Cl Het1 5625 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₃ Cl Het1 5626 SCH₃ SCH₃ CH₃ Cl Het1 5627 SCH₂CH₃ SCH₂CH₃ CH₃ Cl Het1 5628 N(CH₃)₂ N(CH₃)₂ CH₃ Cl Het1 5629 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₃ Cl Het1 5630 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₃ Cl Het1 5631 O—(CH₂CH₂)—O CH₃ Cl Het1 5632 O—(CH₂CH₂CH₂)—O CH₃ Cl Het1 5633 S—(CH₂CH₂)—S CH₃ Cl Het1 5634 S—(CH₂CH₂CH₂)—S CH₃ Cl Het1 5635 —(CH₂)₄— CH₃ Cl Het1 5636 —(CH₂)₅— CH₃ Cl Het1 5637 H H CH₂CH₃ Cl Het1 5638 CH₃ CH₃ CH₂CH₃ Cl Het1 5639 CH₂CH₃ CH₂CH₃ CH₂CH₃ Cl Het1 5640 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₂CH₃ Cl Het1 5641 OCH₃ OCH₃ CH₂CH₃ Cl Het1 5642 OCH₂CH₃ OCH₂CH₃ CH₂CH₃ Cl Het1 5643 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₂CH₃ Cl Het1 5644 SCH₃ SCH₃ CH₂CH₃ Cl Het1 5645 SCH₂CH₃ SCH₂CH₃ CH₂CH₃ Cl Het1 5646 N(CH₃)₂ N(CH₃)₂ CH₂CH₃ Cl Het1 5647 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₂CH₃ Cl Het1 5648 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₂CH₃ Cl Het1 5649 O—(CH₂CH₂)—O CH₂CH₃ Cl Het1 5650 O—(CH₂CH₂CH₂)—O CH₂CH₃ Cl Het1 5651 S—(CH₂CH₂)—S CH₂CH₃ Cl Het1 5652 S—(CH₂CH₂CH₂)—S CH₂CH₃ Cl Het1 5653 —(CH₂)₄— CH₂CH₃ Cl Het1 5654 —(CH₂)₅— CH₂CH₃ Cl Het1 5655 H H CF₃ Cl Het1 5656 CH₃ CH₃ CF₃ Cl Het1 5657 CH₂CH₃ CH₂CH₃ CF₃ Cl Het1 5658 CH₂CH₂CH₃ CH₂CH₂CH₃ CF₃ Cl Het1 5659 OCH₃ OCH₃ CF₃ Cl Het1 5660 OCH₂CH₃ OCH₂CH₃ CF₃ Cl Het1 5661 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CF₃ Cl Het1 5662 SCH₃ SCH₃ CF₃ Cl Het1 5663 SCH₂CH₃ SCH₂CH₃ CF₃ Cl Het1 5664 N(CH₃)₂ N(CH₃)₂ CF₃ Cl Het1 5665 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CF₃ Cl Het1 5666 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CF₃ Cl Het1 5667 O—(CH₂CH₂)—O CF₃ Cl Het1 5668 O—(CH₂CH₂CH₂)—O CF₃ Cl Het1 5669 S—(CH₂CH₂)—S CF₃ Cl Het1 5670 S—(CH₂CH₂CH₂)—S CF₃ Cl Het1 5671 —(CH₂)₄— CF₃ Cl Het1 5672 —(CH₂)₅— CF₃ Cl Het1 5673 H H OCH₃ Cl Het1 5674 CH₃ CH₃ OCH₃ Cl Het1 5675 CH₂CH₃ CH₂CH₃ OCH₃ Cl Het1 5676 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₃ Cl Het1 5677 OCH₃ OCH₃ OCH₃ Cl Het1 5678 OCH₂CH₃ OCH₂CH₃ OCH₃ Cl Het1 5679 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₃ Cl Het1 5680 SCH₃ SCH₃ OCH₃ Cl Het1 5681 SCH₂CH₃ SCH₂CH₃ OCH₃ Cl Het1 5682 N(CH₃)₂ N(CH₃)₂ OCH₃ Cl Het1 5683 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₃ Cl Het1 5684 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₃ Cl Het1 5685 O—(CH₂CH₂)—O OCH₃ Cl Het1 5686 O—(CH₂CH₂CH₂)—O OCH₃ Cl Het1 5687 S—(CH₂CH₂)—S OCH₃ Cl Het1 5688 S—(CH₂CH₂CH₂)—S OCH₃ Cl Het1 5689 —(CH₂)₄— OCH₃ Cl Het1 5690 —(CH₂)₅— OCH₃ Cl Het1 5691 H H OCH₂CH₃ Cl Het1 5692 CH₃ CH₃ OCH₂CH₃ Cl Het1 5693 CH₂CH₃ CH₂CH₃ OCH₂CH₃ Cl Het1 5694 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₂CH₃ Cl Het1 5695 OCH₃ OCH₃ OCH₂CH₃ Cl Het1 5696 OCH₂CH₃ OCH₂CH₃ OCH₂CH₃ Cl Het1 5697 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₂CH₃ Cl Het1 5698 SCH₃ SCH₃ OCH₂CH₃ Cl Het1 5699 SCH₂CH₃ SCH₂CH₃ OCH₂CH₃ Cl Het1 5700 N(CH₃)₂ N(CH₃)₂ OCH₂CH₃ Cl Het1 5701 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₂CH₃ Cl Het1 5702 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₂CH₃ Cl Het1 5703 O—(CH₂CH₂)—O OCH₂CH₃ Cl Het1 5704 O—(CH₂CH₂CH₂)—O OCH₂CH₃ Cl Het1 5705 S—(CH₂CH₂)—S OCH₂CH₃ Cl Het1 5706 S—(CH₂CH₂CH₂)—S OCH₂CH₃ Cl Het1 5707 —(CH₂)₄— OCH₂CH₃ Cl Het1 5708 —(CH₂)₅— OCH₂CH₃ Cl Het1 5709 H H SCH₃ Cl Het1 5710 CH₃ CH₃ SCH₃ Cl Het1 5711 CH₂CH₃ CH₂CH₃ SCH₃ Cl Het1 5712 CH₂CH₂CH₃ CH₂CH₂CH₃ SCH₃ Cl Het1 5713 OCH₃ OCH₃ SCH₃ Cl Het1 5714 OCH₂CH₃ OCH₂CH₃ SCH₃ Cl Het1 5715 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SCH₃ Cl Het1 5716 SCH₃ SCH₃ SCH₃ Cl Het1 5717 SCH₂CH₃ SCH₂CH₃ SCH₃ Cl Het1 5718 N(CH₃)₂ N(CH₃)₂ SCH₃ Cl Het1 5719 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SCH₃ Cl Het1 5720 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SCH₃ Cl Het1 5721 O—(CH₂CH₂)—O SCH₃ Cl Het1 5722 O—(CH₂CH₂CH₂)—O SCH₃ Cl Het1 5723 S—(CH₂CH₂)—S SCH₃ Cl Het1 5724 S—(CH₂CH₂CH₂)—S SCH₃ Cl Het1 5725 —(CH₂)₄— SCH₃ Cl Het1 5726 —(CH₂)₅— SCH₃ Cl Het1 5727 H H SO₂CH₃ Cl Het1 5728 CH₃ CH₃ SO₂CH₃ Cl Het1 5729 CH₂CH₃ CH₂CH₃ SO₂CH₃ Cl Het1 5730 CH₂CH₂CH₃ CH₂CH₂CH₃ SO₂CH₃ Cl Het1 5731 OCH₃ OCH₃ SO₂CH₃ Cl Het1 5732 OCH₂CH₃ OCH₂CH₃ SO₂CH₃ Cl Het1 5733 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SO₂CH₃ Cl Het1 5734 SCH₃ SCH₃ SO₂CH₃ Cl Het1 5735 SCH₂CH₃ SCH₂CH₃ SO₂CH₃ Cl Het1 5736 N(CH₃)₂ N(CH₃)₂ SO₂CH₃ Cl Het1 5737 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SO₂CH₃ Cl Het1 5738 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SO₂CH₃ Cl Het1 5739 O—(CH₂CH₂)—O SO₂CH₃ Cl Het1 5740 O—(CH₂CH₂CH₂)—O SO₂CH₃ Cl Het1 5741 S—(CH₂CH₂)—S SO₂CH₃ Cl Het1 5742 S—(CH₂CH₂CH₂)—S SO₂CH₃ Cl Het1 5743 —(CH₂)₄— SO₂CH₃ Cl Het1 5744 —(CH₂)₅— SO₂CH₃ Cl Het1 5745 H H PO(OCH₃)₂ Cl Het1 5746 CH₃ CH₃ PO(OCH₃)₂ Cl Het1 5747 CH₂CH₃ CH₂CH₃ PO(OCH₃)₂ Cl Het1 5748 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₃)₂ Cl Het1 5749 OCH₃ OCH₃ PO(OCH₃)₂ Cl Het1 5750 OCH₂CH₃ OCH₂CH₃ PO(OCH₃)₂ Cl Het1 5751 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₃)₂ Cl Het1 5752 SCH₃ SCH₃ PO(OCH₃)₂ Cl Het1 5753 SCH₂CH₃ SCH₂CH₃ PO(OCH₃)₂ Cl Het1 5754 N(CH₃)₂ N(CH₃)₂ PO(OCH₃)₂ Cl Het1 5755 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₃)₂ Cl Het1 5756 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₃)₂ Cl Het1 5757 O—(CH₂CH₂)—O PO(OCH₃)₂ Cl Het1 5758 O—(CH₂CH₂CH₂)—O PO(OCH₃)₂ Cl Het1 5759 S—(CH₂CH₂)—S PO(OCH₃)₂ Cl Het1 5760 S—(CH₂CH₂CH₂)—S PO(OCH₃)₂ Cl Het1 5761 —(CH₂)₄— PO(OCH₃)₂ Cl Het1 5762 —(CH₂)₅— PO(OCH₃)₂ Cl Het1 5763 H H PO(OCH₂CH₃)₂ Cl Het1 5764 CH₃ CH₃ PO(OCH₂CH₃)₂ Cl Het1 5765 CH₂CH₃ CH₂CH₃ PO(OCH₂CH₃)₂ Cl Het1 5766 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₂CH₃)₂ Cl Het1 5767 OCH₃ OCH₃ PO(OCH₂CH₃)₂ Cl Het1 5768 OCH₂CH₃ OCH₂CH₃ PO(OCH₂CH₃)₂ Cl Het1 5769 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₂CH₃)₂ Cl Het1 5770 SCH₃ SCH₃ PO(OCH₂CH₃)₂ Cl Het1 5771 SCH₂CH₃ SCH₂CH₃ PO(OCH₂CH₃)₂ Cl Het1 5772 N(CH₃)₂ N(CH₃)₂ PO(OCH₂CH₃)₂ Cl Het1 5773 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₂CH₃)₂ Cl Het1 5774 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₂CH₃)₂ Cl Het1 5775 O—(CH₂CH₂)—O PO(OCH₂CH₃)₂ Cl Het1 5776 O—(CH₂CH₂CH₂)—O PO(OCH₂CH₃)₂ Cl Het1 5777 S—(CH₂CH₂)—S PO(OCH₂CH₃)₂ Cl Het1 5778 S—(CH₂CH₂CH₂)—S PO(OCH₂CH₃)₂ Cl Het1 5779 —(CH₂)₄— PO(OCH₂CH₃)₂ Cl Het1 5780 —(CH₂)₅— PO(OCH₂CH₃)₂ Cl Het1 5781 H H PO(CH₃)₂ Cl Het1 5782 CH₃ CH₃ PO(CH₃)₂ Cl Het1 5783 CH₂CH₃ CH₂CH₃ PO(CH₃)₂ Cl Het1 5784 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₃)₂ Cl Het1 5785 OCH₃ OCH₃ PO(CH₃)₂ Cl Het1 5786 OCH₂CH₃ OCH₂CH₃ PO(CH₃)₂ Cl Het1 5787 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₃)₂ Cl Het1 5788 SCH₃ SCH₃ PO(CH₃)₂ Cl Het1 5789 SCH₂CH₃ SCH₂CH₃ PO(CH₃)₂ Cl Het1 5790 N(CH₃)₂ N(CH₃)₂ PO(CH₃)₂ Cl Het1 5791 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₃)₂ Cl Het1 5792 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₃)₂ Cl Het1 5793 O—(CH₂CH₂)—O PO(CH₃)₂ Cl Het1 5794 O—(CH₂CH₂CH₂)—O PO(CH₃)₂ Cl Het1 5795 S—(CH₂CH₂)—S PO(CH₃)₂ Cl Het1 5796 S—(CH₂CH₂CH₂)—S PO(CH₃)₂ Cl Het1 5797 —(CH₂)₄— PO(CH₃)₂ Cl Het1 5798 —(CH₂)₅— PO(CH₃)₂ Cl Het1 5799 H H PC(CH₂CH₃)₂ Cl Het1 5800 CH₃ CH₃ PC(CH₂CH₃)₂ Cl Het1 5801 CH₂CH₃ CH₂CH₃ PC(CH₂CH₃)₂ Cl Het1 5802 CH₂CH₂CH₃ CH₂CH₂CH₃ PC(CH₂CH₃)₂ Cl Het1 5803 OCH₃ OCH₃ PC(CH₂CH₃)₂ Cl Het1 5804 OCH₂CH₃ OCH₂CH₃ PC(CH₂CH₃)₂ Cl Het1 5805 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PC(CH₂CH₃)₂ Cl Het1 5806 SCH₃ SCH₃ PC(CH₂CH₃)₂ Cl Het1 5807 SCH₂CH₃ SCH₂CH₃ PC(CH₂CH₃)₂ Cl Het1 5808 N(CH₃)₂ N(CH₃)₂ PC(CH₂CH₃)₂ Cl Het1 5809 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PC(CH₂CH₃)₂ Cl Het1 5810 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PC(CH₂CH₃)₂ Cl Het1 5811 O—(CH₂CH₂)—O PC(CH₂CH₃)₂ Cl Het1 5812 O—(CH₂CH₂CH₂)—O PC(CH₂CH₃)₂ Cl Het1 5813 S—(CH₂CH₂)—S PC(CH₂CH₃)₂ Cl Het1 5814 S—(CH₂CH₂CH₂)—S PC(CH₂CH₃)₂ Cl Het1 5815 —(CH₂)₄— PC(CH₂CH₃)₂ Cl Het1 5816 —(CH₂)₅— PC(CH₂CH₃)₂ Cl Het1 5817 H H H Cl Het2 5818 CH₃ CH₃ H Cl Het2 5819 CH₂CH₃ CH₂CH₃ H Cl Het2 5820 CH₂CH₂CH₃ CH₂CH₂CH₃ H Cl Het2 5821 OCH₃ OCH₃ H Cl Het2 5822 OCH₂CH₃ OCH₂CH₃ H Cl Het2 5823 OCH₂CH₂CH₃ OCH₂CH₂CH₃ H Cl Het2 5824 SCH₃ SCH₃ H Cl Het2 5825 SCH₂CH₃ SCH₂CH₃ H Cl Het2 5826 N(CH₃)₂ N(CH₃)₂ H Cl Het2 5827 N(CH₂CH₃)₂ N(CH₂CH₃)₂ H Cl Het2 5828 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) H Cl Het2 5829 O—(CH₂CH₂)—O H Cl Het2 5830 O—(CH₂CH₂CH₂)—O H Cl Het2 5831 S—(CH₂CH₂)—S H Cl Het2 5832 S—(CH₂CH₂CH₂)—S H Cl Het2 5833 —(CH₂)₄— H Cl Het2 5834 —(CH₂)₅— H Cl Het2 5835 H H NO₂ Cl Het2 5836 CH₃ CH₃ NO₂ Cl Het2 5837 CH₂CH₃ CH₂CH₃ NO₂ Cl Het2 5838 CH₂CH₂CH₃ CH₂CH₂CH₃ NO₂ Cl Het2 5839 OCH₃ OCH₃ NO₂ Cl Het2 5840 OCH₂CH₃ OCH₂CH₃ NO₂ Cl Het2 5841 OCH₂CH₂CH₃ OCH₂CH₂CH₃ NO₂ Cl Het2 5842 SCH₃ SCH₃ NO₂ Cl Het2 5843 SCH₂CH₃ SCH₂CH₃ NO₂ Cl Het2 5844 N(CH₃)₂ N(CH₃)₂ NO₂ Cl Het2 5845 N(CH₂CH₃)₂ N(CH₂CH₃)₂ NO₂ Cl Het2 5846 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) NO₂ Cl Het2 5847 O—(CH₂CH₂)—O NO₂ Cl Het2 5848 O—(CH₂CH₂CH₂)—O NO₂ Cl Het2 5849 S—(CH₂CH₂)—S NO₂ Cl Het2 5850 S—(CH₂CH₂CH₂)—S NO₂ Cl Het2 5851 —(CH₂)₄— NO₂ Cl Het2 5852 —(CH₂)₅— NO₂ Cl Het2 5853 H H CN Cl Het2 5854 CH₃ CH₃ CN Cl Het2 5855 CH₂CH₃ CH₂CH₃ CN Cl Het2 5856 CH₂CH₂CH₃ CH₂CH₂CH₃ CN Cl Het2 5857 OCH₃ OCH₃ CN Cl Het2 5858 OCH₂CH₃ OCH₂CH₃ CN Cl Het2 5859 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CN Cl Het2 5860 SCH₃ SCH₃ CN Cl Het2 5861 SCH₂CH₃ SCH₂CH₃ CN Cl Het2 5862 N(CH₃)₂ N(CH₃)₂ CN Cl Het2 5863 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CN Cl Het2 5864 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CN Cl Het2 5865 O—(CH₂CH₂)—O CN Cl Het2 5866 O—(CH₂CH₂CH₂)—O CN Cl Het2 5867 S—(CH₂CH₂)—S CN Cl Het2 5868 S—(CH₂CH₂CH₂)—S CN Cl Het2 5869 —(CH₂)₄— CN Cl Het2 5870 —(CH₂)₅— CN Cl Het2 5871 H H F Cl Het2 5872 CH₃ CH₃ F Cl Het2 5873 CH₂CH₃ CH₂CH₃ F Cl Het2 5874 CH₂CH₂CH₃ CH₂CH₂CH₃ F Cl Het2 5875 OCH₃ OCH₃ F Cl Het2 5876 OCH₂CH₃ OCH₂CH₃ F Cl Het2 5877 OCH₂CH₂CH₃ OCH₂CH₂CH₃ F Cl Het2 5878 SCH₃ SCH₃ F Cl Het2 5879 SCH₂CH₃ SCH₂CH₃ F Cl Het2 5880 N(CH₃)₂ N(CH₃)₂ F Cl Het2 5881 N(CH₂CH₃)₂ N(CH₂CH₃)₂ F Cl Het2 5882 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) F Cl Het2 5883 O—(CH₂CH₂)—O F Cl Het2 5884 O—(CH₂CH₂CH₂)—O F Cl Het2 5885 S—(CH₂CH₂)—S F Cl Het2 5886 S—(CH₂CH₂CH₂)—S F Cl Het2 5887 —(CH₂)₄— F Cl Het2 5888 —(CH₂)₅— F Cl Het2 5889 H H Cl Cl Het2 5890 CH₃ CH₃ Cl Cl Het2 5891 CH₂CH₃ CH₂CH₃ Cl Cl Het2 5892 CH₂CH₂CH₃ CH₂CH₂CH₃ Cl Cl Het2 5893 OCH₃ OCH₃ Cl Cl Het2 5894 OCH₂CH₃ OCH₂CH₃ Cl Cl Het2 5895 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Cl Cl Het2 5896 SCH₃ SCH₃ Cl Cl Het2 5897 SCH₂CH₃ SCH₂CH₃ Cl Cl Het2 5898 N(CH₃)₂ N(CH₃)₂ Cl Cl Het2 5899 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Cl Cl Het2 5900 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Cl Cl Het2 5901 O—(CH₂CH₂)—O Cl Cl Het2 5902 O—(CH₂CH₂CH₂)—O Cl Cl Het2 5903 S—(CH₂CH₂)—S Cl Cl Het2 5904 S—(CH₂CH₂CH₂)—S Cl Cl Het2 5905 —(CH₂)₄— Cl Cl Het2 5906 —(CH₂)₅— Cl Cl Het2 5907 H H Br Cl Het2 5908 CH₃ CH₃ Br Cl Het2 5909 CH₂CH₃ CH₂CH₃ Br Cl Het2 5910 CH₂CH₂CH₃ CH₂CH₂CH₃ Br Cl Het2 5911 OCH₃ OCH₃ Br Cl Het2 5912 OCH₂CH₃ OCH₂CH₃ Br Cl Het2 5913 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Br Cl Het2 5914 SCH₃ SCH₃ Br Cl Het2 5915 SCH₂CH₃ SCH₂CH₃ Br Cl Het2 5916 N(CH₃)₂ N(CH₃)₂ Br Cl Het2 5917 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Br Cl Het2 5918 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Br Cl Het2 5919 O—(CH₂CH₂)—O Br Cl Het2 5920 O—(CH₂CH₂CH₂)—O Br Cl Het2 5921 S—(CH₂CH₂)—S Br Cl Het2 5922 S—(CH₂CH₂CH₂)—S Br Cl Het2 5923 —(CH₂)₄— Br Cl Het2 5924 —(CH₂)₅— Br Cl Het2 5925 H H CH₃ Cl Het2 5926 CH₃ CH₃ CH₃ Cl Het2 5927 CH₂CH₃ CH₂CH₃ CH₃ Cl Het2 5928 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₃ Cl Het2 5929 OCH₃ OCH₃ CH₃ Cl Het2 5930 OCH₂CH₃ OCH₂CH₃ CH₃ Cl Het2 5931 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₃ Cl Het2 5932 SCH₃ SCH₃ CH₃ Cl Het2 5933 SCH₂CH₃ SCH₂CH₃ CH₃ Cl Het2 5934 N(CH₃)₂ N(CH₃)₂ CH₃ Cl Het2 5935 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₃ Cl Het2 5936 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₃ Cl Het2 5937 O—(CH₂CH₂)—O CH₃ Cl Het2 5938 O—(CH₂CH₂CH₂)—O CH₃ Cl Het2 5939 S—(CH₂CH₂)—S CH₃ Cl Het2 5940 S—(CH₂CH₂CH₂)—S CH₃ Cl Het2 5941 —(CH₂)₄— CH₃ Cl Het2 5942 —(CH₂)₅— CH₃ Cl Het2 5943 H H CH₂CH₃ Cl Het2 5944 CH₃ CH₃ CH₂CH₃ Cl Het2 5945 CH₂CH₃ CH₂CH₃ CH₂CH₃ Cl Het2 5946 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₂CH₃ Cl Het2 5947 OCH₃ OCH₃ CH₂CH₃ Cl Het2 5948 OCH₂CH₃ OCH₂CH₃ CH₂CH₃ Cl Het2 5949 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₂CH₃ Cl Het2 5950 SCH₃ SCH₃ CH₂CH₃ Cl Het2 5951 SCH₂CH₃ SCH₂CH₃ CH₂CH₃ Cl Het2 5952 N(CH₃)₂ N(CH₃)₂ CH₂CH₃ Cl Het2 5953 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₂CH₃ Cl Het2 5954 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₂CH₃ Cl Het2 5955 O—(CH₂CH₂)—O CH₂CH₃ Cl Het2 5956 O—(CH₂CH₂CH₂)—O CH₂CH₃ Cl Het2 5957 S—(CH₂CH₂)—S CH₂CH₃ Cl Het2 5958 S—(CH₂CH₂CH₂)—S CH₂CH₃ Cl Het2 5959 —(CH₂)₄— CH₂CH₃ Cl Het2 5960 —(CH₂)₅— CH₂CH₃ Cl Het2 5961 H H CF₃ Cl Het2 5962 CH₃ CH₃ CF₃ Cl Het2 5963 CH₂CH₃ CH₂CH₃ CF₃ Cl Het2 5964 CH₂CH₂CH₃ CH₂CH₂CH₃ CF₃ Cl Het2 5965 OCH₃ OCH₃ CF₃ Cl Het2 5966 OCH₂CH₃ OCH₂CH₃ CF₃ Cl Het2 5967 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CF₃ Cl Het2 5968 SCH₃ SCH₃ CF₃ Cl Het2 5969 SCH₂CH₃ SCH₂CH₃ CF₃ Cl Het2 5970 N(CH₃)₂ N(CH₃)₂ CF₃ Cl Het2 5971 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CF₃ Cl Het2 5972 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CF₃ Cl Het2 5973 O—(CH₂CH₂)—O CF₃ Cl Het2 5974 O—(CH₂CH₂CH₂)—O CF₃ Cl Het2 5975 S—(CH₂CH₂)—S CF₃ Cl Het2 5976 S—(CH₂CH₂CH₂)—S CF₃ Cl Het2 5977 —(CH₂)₄— CF₃ Cl Het2 5978 —(CH₂)₅— CF₃ Cl Het2 5979 H H OCH₃ Cl Het2 5980 CH₃ CH₃ OCH₃ Cl Het2 5981 CH₂CH₃ CH₂CH₃ OCH₃ Cl Het2 5982 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₃ Cl Het2 5983 OCH₃ OCH₃ OCH₃ Cl Het2 5984 OCH₂CH₃ OCH₂CH₃ OCH₃ Cl Het2 5985 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₃ Cl Het2 5986 SCH₃ SCH₃ OCH₃ Cl Het2 5987 SCH₂CH₃ SCH₂CH₃ OCH₃ Cl Het2 5988 N(CH₃)₂ N(CH₃)₂ OCH₃ Cl Het2 5989 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₃ Cl Het2 5990 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₃ Cl Het2 5991 O—(CH₂CH₂)—O OCH₃ Cl Het2 5992 O—(CH₂CH₂CH₂)—O OCH₃ Cl Het2 5993 S—(CH₂CH₂)—S OCH₃ Cl Het2 5994 S—(CH₂CH₂CH₂)—S OCH₃ Cl Het2 5995 —(CH₂)₄— OCH₃ Cl Het2 5996 —(CH₂)₅— OCH₃ Cl Het2 5997 H H OCH₂CH₃ Cl Het2 5998 CH₃ CH₃ OCH₂CH₃ Cl Het2 5999 CH₂CH₃ CH₂CH₃ OCH₂CH₃ Cl Het2 6000 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₂CH₃ Cl Het2 6001 OCH₃ OCH₃ OCH₂CH₃ Cl Het2 6002 OCH₂CH₃ OCH₂CH₃ OCH₂CH₃ Cl Het2 6003 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₂CH₃ Cl Het2 6004 SCH₃ SCH₃ OCH₂CH₃ Cl Het2 6005 SCH₂CH₃ SCH₂CH₃ OCH₂CH₃ Cl Het2 6006 N(CH₃)₂ N(CH₃)₂ OCH₂CH₃ Cl Het2 6007 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₂CH₃ Cl Het2 6008 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₂CH₃ Cl Het2 6009 O—(CH₂CH₂)—O OCH₂CH₃ Cl Het2 6010 O—(CH₂CH₂CH₂)—O OCH₂CH₃ Cl Het2 6011 S—(CH₂CH₂)—S OCH₂CH₃ Cl Het2 6012 S—(CH₂CH₂CH₂)—S OCH₂CH₃ Cl Het2 6013 —(CH₂)₄— OCH₂CH₃ Cl Het2 6014 —(CH₂)₅— OCH₂CH₃ Cl Het2 6015 H H SCH₃ Cl Het2 6016 CH₃ CH₃ SCH₃ Cl Het2 6017 CH₂CH₃ CH₂CH₃ SCH₃ Cl Het2 6018 CH₂CH₂CH₃ CH₂CH₂CH₃ SCH₃ Cl Het2 6019 OCH₃ OCH₃ SCH₃ Cl Het2 6020 OCH₂CH₃ OCH₂CH₃ SCH₃ Cl Het2 6021 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SCH₃ Cl Het2 6022 SCH₃ SCH₃ SCH₃ Cl Het2 6023 SCH₂CH₃ SCH₂CH₃ SCH₃ Cl Het2 6024 N(CH₃)₂ N(CH₃)₂ SCH₃ Cl Het2 6025 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SCH₃ Cl Het2 6026 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SCH₃ Cl Het2 6027 O—(CH₂CH₂)—O SCH₃ Cl Het2 6028 O—(CH₂CH₂CH₂)—O SCH₃ Cl Het2 6029 S—(CH₂CH₂)—S SCH₃ Cl Het2 6030 S—(CH₂CH₂CH₂)—S SCH₃ Cl Het2 6031 —(CH₂)₄— SCH₃ Cl Het2 6032 —(CH₂)₅— SCH₃ Cl Het2 6033 H H SO₂CH₃ Cl Het2 6034 CH₃ CH₃ SO₂CH₃ Cl Het2 6035 CH₂CH₃ CH₂CH₃ SO₂CH₃ Cl Het2 6036 CH₂CH₂CH₃ CH₂CH₂CH₃ SO₂CH₃ Cl Het2 6037 OCH₃ OCH₃ SO₂CH₃ Cl Het2 6038 OCH₂CH₃ OCH₂CH₃ SO₂CH₃ Cl Het2 6039 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SO₂CH₃ Cl Het2 6040 SCH₃ SCH₃ SO₂CH₃ Cl Het2 6041 SCH₂CH₃ SCH₂CH₃ SO₂CH₃ Cl Het2 6042 N(CH₃)₂ N(CH₃)₂ SO₂CH₃ Cl Het2 6043 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SO₂CH₃ Cl Het2 6044 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SO₂CH₃ Cl Het2 6045 O—(CH₂CH₂)—O SO₂CH₃ Cl Het2 6046 O—(CH₂CH₂CH₂)—O SO₂CH₃ Cl Het2 6047 S—(CH₂CH₂)—S SO₂CH₃ Cl Het2 6048 S—(CH₂CH₂CH₂)—S SO₂CH₃ Cl Het2 6049 —(CH₂)₄— SO₂CH₃ Cl Het2 6050 —(CH₂)₅— SO₂CH₃ Cl Het2 6051 H H PO(OCH₃)₂ Cl Het2 6052 CH₃ CH₃ PO(OCH₃)₂ Cl Het2 6053 CH₂CH₃ CH₂CH₃ PO(OCH₃)₂ Cl Het2 6054 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₃)₂ Cl Het2 6055 OCH₃ OCH₃ PO(OCH₃)₂ Cl Het2 6056 OCH₂CH₃ OCH₂CH₃ PO(OCH₃)₂ Cl Het2 6057 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₃)₂ Cl Het2 6058 SCH₃ SCH₃ PO(OCH₃)₂ Cl Het2 6059 SCH₂CH₃ SCH₂CH₃ PO(OCH₃)₂ Cl Het2 6060 N(CH₃)₂ N(CH₃)₂ PO(OCH₃)₂ Cl Het2 6061 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₃)₂ Cl Het2 6062 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₃)₂ Cl Het2 6063 O—(CH₂CH₂)—O PO(OCH₃)₂ Cl Het2 6064 O—(CH₂CH₂CH₂)—O PO(OCH₃)₂ Cl Het2 6065 S—(CH₂CH₂)—S PO(OCH₃)₂ Cl Het2 6066 S—(CH₂CH₂CH₂)—S PO(OCH₃)₂ Cl Het2 6067 —(CH₂)₄— PO(OCH₃)₂ Cl Het2 6068 —(CH₂)₅— PO(OCH₃)₂ Cl Het2 6069 H H PO(OCH₂CH₃)₂ Cl Het2 6070 CH₃ CH₃ PO(OCH₂CH₃)₂ Cl Het2 6071 CH₂CH₃ CH₂CH₃ PO(OCH₂CH₃)₂ Cl Het2 6072 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₂CH₃)₂ Cl Het2 6073 OCH₃ OCH₃ PO(OCH₂CH₃)₂ Cl Het2 6074 OCH₂CH₃ OCH₂CH₃ PO(OCH₂CH₃)₂ Cl Het2 6075 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₂CH₃)₂ Cl Het2 6076 SCH₃ SCH₃ PO(OCH₂CH₃)₂ Cl Het2 6077 SCH₂CH₃ SCH₂CH₃ PO(OCH₂CH₃)₂ Cl Het2 6078 N(CH₃)₂ N(CH₃)₂ PO(OCH₂CH₃)₂ Cl Het2 6079 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₂CH₃)₂ Cl Het2 6080 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₂CH₃)₂ Cl Het2 6081 O—(CH₂CH₂)—O PO(OCH₂CH₃)₂ Cl Het2 6082 O—(CH₂CH₂CH₂)—O PO(OCH₂CH₃)₂ Cl Het2 6083 S—(CH₂CH₂)—S PO(OCH₂CH₃)₂ Cl Het2 6084 S—(CH₂CH₂CH₂)—S PO(OCH₂CH₃)₂ Cl Het2 6085 —(CH₂)₄— PO(OCH₂CH₃)₂ Cl Het2 6086 —(CH₂)₅— PO(OCH₂CH₃)₂ Cl Het2 6087 H H PO(CH₃)₂ Cl Het2 6088 CH₃ CH₃ PO(CH₃)₂ Cl Het2 6089 CH₂CH₃ CH₂CH₃ PO(CH₃)₂ Cl Het2 6090 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₃)₂ Cl Het2 6091 OCH₃ OCH₃ PO(CH₃)₂ Cl Het2 6092 OCH₂CH₃ OCH₂CH₃ PO(CH₃)₂ Cl Het2 6093 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₃)₂ Cl Het2 6094 SCH₃ SCH₃ PO(CH₃)₂ Cl Het2 6095 SCH₂CH₃ SCH₂CH₃ PO(CH₃)₂ Cl Het2 6096 N(CH₃)₂ N(CH₃)₂ PO(CH₃)₂ Cl Het2 6097 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₃)₂ Cl Het2 6098 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₃)₂ Cl Het2 6099 O—(CH₂CH₂)—O PO(CH₃)₂ Cl Het2 6100 O—(CH₂CH₂CH₂)—O PO(CH₃)₂ Cl Het2 6101 S—(CH₂CH₂)—S PO(CH₃)₂ Cl Het2 6102 S—(CH₂CH₂CH₂)—S PO(CH₃)₂ Cl Het2 6103 —(CH₂)₄— PO(CH₃)₂ Cl Het2 6104 —(CH₂)₅— PO(CH₃)₂ Cl Het2 6105 H H PC(CH₂CH₃)₂ Cl Het2 6106 CH₃ CH₃ PC(CH₂CH₃)₂ Cl Het2 6107 CH₂CH₃ CH₂CH₃ PC(CH₂CH₃)₂ Cl Het2 6108 CH₂CH₂CH₃ CH₂CH₂CH₃ PC(CH₂CH₃)₂ Cl Het2 6109 OCH₃ OCH₃ PC(CH₂CH₃)₂ Cl Het2 6110 OCH₂CH₃ OCH₂CH₃ PC(CH₂CH₃)₂ Cl Het2 6111 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PC(CH₂CH₃)₂ Cl Het2 6112 SCH₃ SCH₃ PC(CH₂CH₃)₂ Cl Het2 6113 SCH₂CH₃ SCH₂CH₃ PC(CH₂CH₃)₂ Cl Het2 6114 N(CH₃)₂ N(CH₃)₂ PC(CH₂CH₃)₂ Cl Het2 6115 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PC(CH₂CH₃)₂ Cl Het2 6116 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PC(CH₂CH₃)₂ Cl Het2 6117 O—(CH₂CH₂)—O PC(CH₂CH₃)₂ Cl Het2 6118 O—(CH₂CH₂CH₂)—O PC(CH₂CH₃)₂ Cl Het2 6119 S—(CH₂CH₂)—S PC(CH₂CH₃)₂ Cl Het2 6120 S—(CH₂CH₂CH₂)—S PC(CH₂CH₃)₂ Cl Het2 6121 —(CH₂)₄— PC(CH₂CH₃)₂ Cl Het2 6122 —(CH₂)₅— PC(CH₂CH₃)₂ Cl Het2 6123 H H H Cl Het3 6124 CH₃ CH₃ H Cl Het3 6125 CH₂CH₃ CH₂CH₃ H Cl Het3 6126 CH₂CH₂CH₃ CH₂CH₂CH₃ H Cl Het3 6127 OCH₃ OCH₃ H Cl Het3 6128 OCH₂CH₃ OCH₂CH₃ H Cl Het3 6129 OCH₂CH₂CH₃ OCH₂CH₂CH₃ H Cl Het3 6130 SCH₃ SCH₃ H Cl Het3 6131 SCH₂CH₃ SCH₂CH₃ H Cl Het3 6132 N(CH₃)₂ N(CH₃)₂ H Cl Het3 6133 N(CH₂CH₃)₂ N(CH₂CH₃)₂ H Cl Het3 6134 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) H Cl Het3 6135 O—(CH₂CH₂)—O H Cl Het3 6136 O—(CH₂CH₂CH₂)—O H Cl Het3 6137 S—(CH₂CH₂)—S H Cl Het3 6138 S—(CH₂CH₂CH₂)—S H Cl Het3 6139 —(CH₂)₄— H Cl Het3 6140 —(CH₂)₅— H Cl Het3 6141 H H NO₂ Cl Het3 6142 CH₃ CH₃ NO₂ Cl Het3 6143 CH₂CH₃ CH₂CH₃ NO₂ Cl Het3 6144 CH₂CH₂CH₃ CH₂CH₂CH₃ NO₂ Cl Het3 6145 OCH₃ OCH₃ NO₂ Cl Het3 6146 OCH₂CH₃ OCH₂CH₃ NO₂ Cl Het3 6147 OCH₂CH₂CH₃ OCH₂CH₂CH₃ NO₂ Cl Het3 6148 SCH₃ SCH₃ NO₂ Cl Het3 6149 SCH₂CH₃ SCH₂CH₃ NO₂ Cl Het3 6150 N(CH₃)₂ N(CH₃)₂ NO₂ Cl Het3 6151 N(CH₂CH₃)₂ N(CH₂CH₃)₂ NO₂ Cl Het3 6152 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) NO₂ Cl Het3 6153 O—(CH₂CH₂)—O NO₂ Cl Het3 6154 O—(CH₂CH₂CH₂)—O NO₂ Cl Het3 6155 S—(CH₂CH₂)—S NO₂ Cl Het3 6156 S—(CH₂CH₂CH₂)—S NO₂ Cl Het3 6157 —(CH₂)₄— NO₂ Cl Het3 6158 —(CH₂)₅— NO₂ Cl Het3 6159 H H CN Cl Het3 6160 CH₃ CH₃ CN Cl Het3 6161 CH₂CH₃ CH₂CH₃ CN Cl Het3 6162 CH₂CH₂CH₃ CH₂CH₂CH₃ CN Cl Het3 6163 OCH₃ OCH₃ CN Cl Het3 6164 OCH₂CH₃ OCH₂CH₃ CN Cl Het3 6165 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CN Cl Het3 6166 SCH₃ SCH₃ CN Cl Het3 6167 SCH₂CH₃ SCH₂CH₃ CN Cl Het3 6168 N(CH₃)₂ N(CH₃)₂ CN Cl Het3 6169 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CN Cl Het3 6170 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CN Cl Het3 6171 O—(CH₂CH₂)—O CN Cl Het3 6172 O—(CH₂CH₂CH₂)—O CN Cl Het3 6173 S—(CH₂CH₂)—S CN Cl Het3 6174 S—(CH₂CH₂CH₂)—S CN Cl Het3 6175 —(CH₂)₄— CN Cl Het3 6176 —(CH₂)₅— CN Cl Het3 6177 H H F Cl Het3 6178 CH₃ CH₃ F Cl Het3 6179 CH₂CH₃ CH₂CH₃ F Cl Het3 6180 CH₂CH₂CH₃ CH₂CH₂CH₃ F Cl Het3 6181 OCH₃ OCH₃ F Cl Het3 6182 OCH₂CH₃ OCH₂CH₃ F Cl Het3 6183 OCH₂CH₂CH₃ OCH₂CH₂CH₃ F Cl Het3 6184 SCH₃ SCH₃ F Cl Het3 6185 SCH₂CH₃ SCH₂CH₃ F Cl Het3 6186 N(CH₃)₂ N(CH₃)₂ F Cl Het3 6187 N(CH₂CH₃)₂ N(CH₂CH₃)₂ F Cl Het3 6188 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) F Cl Het3 6189 O—(CH₂CH₂)—O F Cl Het3 6190 O—(CH₂CH₂CH₂)—O F Cl Het3 6191 S—(CH₂CH₂)—S F Cl Het3 6192 S—(CH₂CH₂CH₂)—S F Cl Het3 6193 —(CH₂)₄— F Cl Het3 6194 —(CH₂)₅— F Cl Het3 6195 H H Cl Cl Het3 6196 CH₃ CH₃ Cl Cl Het3 6197 CH₂CH₃ CH₂CH₃ Cl Cl Het3 6198 CH₂CH₂CH₃ CH₂CH₂CH₃ Cl Cl Het3 6199 OCH₃ OCH₃ Cl Cl Het3 6200 OCH₂CH₃ OCH₂CH₃ Cl Cl Het3 6201 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Cl Cl Het3 6202 SCH₃ SCH₃ Cl Cl Het3 6203 SCH₂CH₃ SCH₂CH₃ Cl Cl Het3 6204 N(CH₃)₂ N(CH₃)₂ Cl Cl Het3 6205 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Cl Cl Het3 6206 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Cl Cl Het3 6207 O—(CH₂CH₂)—O Cl Cl Het3 6208 O—(CH₂CH₂CH₂)—O Cl Cl Het3 6209 S—(CH₂CH₂)—S Cl Cl Het3 6210 S—(CH₂CH₂CH₂)—S Cl Cl Het3 6211 —(CH₂)₄— Cl Cl Het3 6212 —(CH₂)₅— Cl Cl Het3 6213 H H Br Cl Het3 6214 CH₃ CH₃ Br Cl Het3 6215 CH₂CH₃ CH₂CH₃ Br Cl Het3 6216 CH₂CH₂CH₃ CH₂CH₂CH₃ Br Cl Het3 6217 OCH₃ OCH₃ Br Cl Het3 6218 OCH₂CH₃ OCH₂CH₃ Br Cl Het3 6219 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Br Cl Het3 6220 SCH₃ SCH₃ Br Cl Het3 6221 SCH₂CH₃ SCH₂CH₃ Br Cl Het3 6222 N(CH₃)₂ N(CH₃)₂ Br Cl Het3 6223 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Br Cl Het3 6224 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Br Cl Het3 6225 O—(CH₂CH₂)—O Br Cl Het3 6226 O—(CH₂CH₂CH₂)—O Br Cl Het3 6227 S—(CH₂CH₂)—S Br Cl Het3 6228 S—(CH₂CH₂CH₂)—S Br Cl Het3 6229 —(CH₂)₄— Br Cl Het3 6230 —(CH₂)₅— Br Cl Het3 6231 H H CH₃ Cl Het3 6232 CH₃ CH₃ CH₃ Cl Het3 6233 CH₂CH₃ CH₂CH₃ CH₃ Cl Het3 6234 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₃ Cl Het3 6235 OCH₃ OCH₃ CH₃ Cl Het3 6236 OCH₂CH₃ OCH₂CH₃ CH₃ Cl Het3 6237 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₃ Cl Het3 6238 SCH₃ SCH₃ CH₃ Cl Het3 6239 SCH₂CH₃ SCH₂CH₃ CH₃ Cl Het3 6240 N(CH₃)₂ N(CH₃)₂ CH₃ Cl Het3 6241 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₃ Cl Het3 6242 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₃ Cl Het3 6243 O—(CH₂CH₂)—O CH₃ Cl Het3 6244 O—(CH₂CH₂CH₂)—O CH₃ Cl Het3 6245 S—(CH₂CH₂)—S CH₃ Cl Het3 6246 S—(CH₂CH₂CH₂)—S CH₃ Cl Het3 6247 —(CH₂)₄— CH₃ Cl Het3 6248 —(CH₂)₅— CH₃ Cl Het3 6249 H H CH₂CH₃ Cl Het3 6250 CH₃ CH₃ CH₂CH₃ Cl Het3 6251 CH₂CH₃ CH₂CH₃ CH₂CH₃ Cl Het3 6252 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₂CH₃ Cl Het3 6253 OCH₃ OCH₃ CH₂CH₃ Cl Het3 6254 OCH₂CH₃ OCH₂CH₃ CH₂CH₃ Cl Het3 6255 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₂CH₃ Cl Het3 6256 SCH₃ SCH₃ CH₂CH₃ Cl Het3 6257 SCH₂CH₃ SCH₂CH₃ CH₂CH₃ Cl Het3 6258 N(CH₃)₂ N(CH₃)₂ CH₂CH₃ Cl Het3 6259 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₂CH₃ Cl Het3 6260 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₂CH₃ Cl Het3 6261 O—(CH₂CH₂)—O CH₂CH₃ Cl Het3 6262 O—(CH₂CH₂CH₂)—O CH₂CH₃ Cl Het3 6263 S—(CH₂CH₂)—S CH₂CH₃ Cl Het3 6264 S—(CH₂CH₂CH₂)—S CH₂CH₃ Cl Het3 6265 —(CH₂)₄— CH₂CH₃ Cl Het3 6266 —(CH₂)₅— CH₂CH₃ Cl Het3 6267 H H CF₃ Cl Het3 6268 CH₃ CH₃ CF₃ Cl Het3 6269 CH₂CH₃ CH₂CH₃ CF₃ Cl Het3 6270 CH₂CH₂CH₃ CH₂CH₂CH₃ CF₃ Cl Het3 6271 OCH₃ OCH₃ CF₃ Cl Het3 6272 OCH₂CH₃ OCH₂CH₃ CF₃ Cl Het3 6273 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CF₃ Cl Het3 6274 SCH₃ SCH₃ CF₃ Cl Het3 6275 SCH₂CH₃ SCH₂CH₃ CF₃ Cl Het3 6276 N(CH₃)₂ N(CH₃)₂ CF₃ Cl Het3 6277 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CF₃ Cl Het3 6278 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CF₃ Cl Het3 6279 O—(CH₂CH₂)—O CF₃ Cl Het3 6280 O—(CH₂CH₂CH₂)—O CF₃ Cl Het3 6281 S—(CH₂CH₂)—S CF₃ Cl Het3 6282 S—(CH₂CH₂CH₂)—S CF₃ Cl Het3 6283 —(CH₂)₄— CF₃ Cl Het3 6284 —(CH₂)₅— CF₃ Cl Het3 6285 H H OCH₃ Cl Het3 6286 CH₃ CH₃ OCH₃ Cl Het3 6287 CH₂CH₃ CH₂CH₃ OCH₃ Cl Het3 6288 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₃ Cl Het3 6289 OCH₃ OCH₃ OCH₃ Cl Het3 6290 OCH₂CH₃ OCH₂CH₃ OCH₃ Cl Het3 6291 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₃ Cl Het3 6292 SCH₃ SCH₃ OCH₃ Cl Het3 6293 SCH₂CH₃ SCH₂CH₃ OCH₃ Cl Het3 6294 N(CH₃)₂ N(CH₃)₂ OCH₃ Cl Het3 6295 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₃ Cl Het3 6296 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₃ Cl Het3 6297 O—(CH₂CH₂)—O OCH₃ Cl Het3 6298 O—(CH₂CH₂CH₂)—O OCH₃ Cl Het3 6299 S—(CH₂CH₂)—S OCH₃ Cl Het3 6300 S—(CH₂CH₂CH₂)—S OCH₃ Cl Het3 6301 —(CH₂)₄— OCH₃ Cl Het3 6302 —(CH₂)₅— OCH₃ Cl Het3 6303 H H OCH₂CH₃ Cl Het3 6304 CH₃ CH₃ OCH₂CH₃ Cl Het3 6305 CH₂CH₃ CH₂CH₃ OCH₂CH₃ Cl Het3 6306 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₂CH₃ Cl Het3 6307 OCH₃ OCH₃ OCH₂CH₃ Cl Het3 6308 OCH₂CH₃ OCH₂CH₃ OCH₂CH₃ Cl Het3 6309 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₂CH₃ Cl Het3 6310 SCH₃ SCH₃ OCH₂CH₃ Cl Het3 6311 SCH₂CH₃ SCH₂CH₃ OCH₂CH₃ Cl Het3 6312 N(CH₃)₂ N(CH₃)₂ OCH₂CH₃ Cl Het3 6313 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₂CH₃ Cl Het3 6314 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₂CH₃ Cl Het3 6315 O—(CH₂CH₂)—O OCH₂CH₃ Cl Het3 6316 O—(CH₂CH₂CH₂)—O OCH₂CH₃ Cl Het3 6317 S—(CH₂CH₂)—S OCH₂CH₃ Cl Het3 6318 S—(CH₂CH₂CH₂)—S OCH₂CH₃ Cl Het3 6319 —(CH₂)₄— OCH₂CH₃ Cl Het3 6320 —(CH₂)₅— OCH₂CH₃ Cl Het3 6331 H H SCH₃ Cl Het3 6332 CH₃ CH₃ SCH₃ Cl Het3 6333 CH₂CH₃ CH₂CH₃ SCH₃ Cl Het3 6334 CH₂CH₂CH₃ CH₂CH₂CH₃ SCH₃ Cl Het3 6335 OCH₃ OCH₃ SCH₃ Cl Het3 6336 OCH₂CH₃ OCH₂CH₃ SCH₃ Cl Het3 6337 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SCH₃ Cl Het3 6338 SCH₃ SCH₃ SCH₃ Cl Het3 6339 SCH₂CH₃ SCH₂CH₃ SCH₃ Cl Het3 6340 N(CH₃)₂ N(CH₃)₂ SCH₃ Cl Het3 6341 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SCH₃ Cl Het3 6342 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SCH₃ Cl Het3 6343 O—(CH₂CH₂)—O SCH₃ Cl Het3 6344 O—(CH₂CH₂CH₂)—O SCH₃ Cl Het3 6345 S—(CH₂CH₂)—S SCH₃ Cl Het3 6346 S—(CH₂CH₂CH₂)—S SCH₃ Cl Het3 6347 —(CH₂)₄— SCH₃ Cl Het3 6348 —(CH₂)₅— SCH₃ Cl Het3 6349 H H SO₂CH₃ Cl Het3 6350 CH₃ CH₃ SO₂CH₃ Cl Het3 6351 CH₂CH₃ CH₂CH₃ SO₂CH₃ Cl Het3 6352 CH₂CH₂CH₃ CH₂CH₂CH₃ SO₂CH₃ Cl Het3 6353 OCH₃ OCH₃ SO₂CH₃ Cl Het3 6354 OCH₂CH₃ OCH₂CH₃ SO₂CH₃ Cl Het3 6355 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SO₂CH₃ Cl Het3 6356 SCH₃ SCH₃ SO₂CH₃ Cl Het3 6357 SCH₂CH₃ SCH₂CH₃ SO₂CH₃ Cl Het3 6358 N(CH₃)₂ N(CH₃)₂ SO₂CH₃ Cl Het3 6359 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SO₂CH₃ Cl Het3 6360 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SO₂CH₃ Cl Het3 6361 O—(CH₂CH₂)—O SO₂CH₃ Cl Het3 6362 O—(CH₂CH₂CH₂)—O SO₂CH₃ Cl Het3 6363 S—(CH₂CH₂)—S SO₂CH₃ Cl Het3 6364 S—(CH₂CH₂CH₂)—S SO₂CH₃ Cl Het3 6365 —(CH₂)₄— SO₂CH₃ Cl Het3 6366 —(CH₂)₅— SO₂CH₃ Cl Het3 6367 H H PO(OCH₃)₂ Cl Het3 6368 CH₃ CH₃ PO(OCH₃)₂ Cl Het3 6369 CH₂CH₃ CH₂CH₃ PO(OCH₃)₂ Cl Het3 6370 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₃)₂ Cl Het3 6371 OCH₃ OCH₃ PO(OCH₃)₂ Cl Het3 6372 OCH₂CH₃ OCH₂CH₃ PO(OCH₃)₂ Cl Het3 6373 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₃)₂ Cl Het3 6374 SCH₃ SCH₃ PO(OCH₃)₂ Cl Het3 6375 SCH₂CH₃ SCH₂CH₃ PO(OCH₃)₂ Cl Het3 6376 N(CH₃)₂ N(CH₃)₂ PO(OCH₃)₂ Cl Het3 6377 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₃)₂ Cl Het3 6378 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₃)₂ Cl Het3 6379 O—(CH₂CH₂)—O PO(OCH₃)₂ Cl Het3 6380 O—(CH₂CH₂CH₂)—O PO(OCH₃)₂ Cl Het3 6381 S—(CH₂CH₂)—S PO(OCH₃)₂ Cl Het3 6382 S—(CH₂CH₂CH₂)—S PO(OCH₃)₂ Cl Het3 6383 —(CH₂)₄— PO(OCH₃)₂ Cl Het3 6384 —(CH₂)₅— PO(OCH₃)₂ Cl Het3 6385 H H PO(OCH₂CH₃)₂ Cl Het3 6386 CH₃ CH₃ PO(OCH₂CH₃)₂ Cl Het3 6387 CH₂CH₃ CH₂CH₃ PO(OCH₂CH₃)₂ Cl Het3 6388 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₂CH₃)₂ Cl Het3 6389 OCH₃ OCH₃ PO(OCH₂CH₃)₂ Cl Het3 6390 OCH₂CH₃ OCH₂CH₃ PO(OCH₂CH₃)₂ Cl Het3 6391 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₂CH₃)₂ Cl Het3 6392 SCH₃ SCH₃ PO(OCH₂CH₃)₂ Cl Het3 6393 SCH₂CH₃ SCH₂CH₃ PO(OCH₂CH₃)₂ Cl Het3 6394 N(CH₃)₂ N(CH₃)₂ PO(OCH₂CH₃)₂ Cl Het3 6395 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₂CH₃)₂ Cl Het3 6396 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₂CH₃)₂ Cl Het3 6397 O—(CH₂CH₂)—O PO(OCH₂CH₃)₂ Cl Het3 6398 O—(CH₂CH₂CH₂)—O PO(OCH₂CH₃)₂ Cl Het3 6399 S—(CH₂CH₂)—S PO(OCH₂CH₃)₂ Cl Het3 6400 S—(CH₂CH₂CH₂)—S PO(OCH₂CH₃)₂ Cl Het3 6401 —(CH₂)₄— PO(OCH₂CH₃)₂ Cl Het3 6402 —(CH₂)₅— PO(OCH₂CH₃)₂ Cl Het3 6403 H H PO(CH₃)₂ Cl Het3 6404 CH₃ CH₃ PO(CH₃)₂ Cl Het3 6405 CH₂CH₃ CH₂CH₃ PO(CH₃)₂ Cl Het3 6406 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₃)₂ Cl Het3 6407 OCH₃ OCH₃ PO(CH₃)₂ Cl Het3 6408 OCH₂CH₃ OCH₂CH₃ PO(CH₃)₂ Cl Het3 6409 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₃)₂ Cl Het3 6410 SCH₃ SCH₃ PO(CH₃)₂ Cl Het3 6411 SCH₂CH₃ SCH₂CH₃ PO(CH₃)₂ Cl Het3 6412 N(CH₃)₂ N(CH₃)₂ PO(CH₃)₂ Cl Het3 6413 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₃)₂ Cl Het3 6414 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₃)₂ Cl Het3 6415 O—(CH₂CH₂)—O PO(CH₃)₂ Cl Het3 6416 O—(CH₂CH₂CH₂)—O PO(CH₃)₂ Cl Het3 6417 S—(CH₂CH₂)—S PO(CH₃)₂ Cl Het3 6418 S—(CH₂CH₂CH₂)—S PO(CH₃)₂ Cl Het3 6419 —(CH₂)₄— PO(CH₃)₂ Cl Het3 6420 —(CH₂)₅— PO(CH₃)₂ Cl Het3 6421 H H PC(CH₂CH₃)₂ Cl Het3 6422 CH₃ CH₃ PC(CH₂CH₃)₂ Cl Het3 6423 CH₂CH₃ CH₂CH₃ PC(CH₂CH₃)₂ Cl Het3 6424 CH₂CH₂CH₃ CH₂CH₂CH₃ PC(CH₂CH₃)₂ Cl Het3 6425 OCH₃ OCH₃ PC(CH₂CH₃)₂ Cl Het3 6426 OCH₂CH₃ OCH₂CH₃ PC(CH₂CH₃)₂ Cl Het3 6427 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PC(CH₂CH₃)₂ Cl Het3 6428 SCH₃ SCH₃ PC(CH₂CH₃)₂ Cl Het3 6429 SCH₂CH₃ SCH₂CH₃ PC(CH₂CH₃)₂ Cl Het3 6430 N(CH₃)₂ N(CH₃)₂ PC(CH₂CH₃)₂ Cl Het3 6431 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PC(CH₂CH₃)₂ Cl Het3 6432 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PC(CH₂CH₃)₂ Cl Het3 6433 O—(CH₂CH₂)—O PC(CH₂CH₃)₂ Cl Het3 6434 O—(CH₂CH₂CH₂)—O PC(CH₂CH₃)₂ Cl Het3 6435 S—(CH₂CH₂)—S PC(CH₂CH₃)₂ Cl Het3 6436 S—(CH₂CH₂CH₂)—S PC(CH₂CH₃)₂ Cl Het3 6437 —(CH₂)₄— PC(CH₂CH₃)₂ Cl Het3 6438 —(CH₂)₅— PC(CH₂CH₃)₂ Cl Het3 6439 H H H Br OH 6440 CH₃ CH₃ H Br OH 6441 CH₂CH₃ CH₂CH₃ H Br OH 6442 CH₂CH₂CH₃ CH₂CH₂CH₃ H Br OH 6443 OCH₃ OCH₃ H Br OH 6444 OCH₂CH₃ OCH₂CH₃ H Br OH 6445 OCH₂CH₂CH₃ OCH₂CH₂CH₃ H Br OH 6446 SCH₃ SCH₃ H Br OH 6447 SCH₂CH₃ SCH₂CH₃ H Br OH 6448 N(CH₃)₂ N(CH₃)₂ H Br OH 6449 N(CH₂CH₃)₂ N(CH₂CH₃)₂ H Br OH 6450 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) H Br OH 6451 O—(CH₂CH₂)—O H Br OH 6452 O—(CH₂CH₂CH₂)—O H Br OH 6453 S—(CH₂CH₂)—S H Br OH 6454 S—(CH₂CH₂CH₂)—S H Br OH 6455 —(CH₂)₄— H Br OH 6456 —(CH₂)₅— H Br OH 6457 H H NO₂ Br OH 6458 CH₃ CH₃ NO₂ Br OH 6459 CH₂CH₃ CH₂CH₃ NO₂ Br OH 6460 CH₂CH₂CH₃ CH₂CH₂CH₃ NO₂ Br OH 6461 OCH₃ OCH₃ NO₂ Br OH 6462 OCH₂CH₃ OCH₂CH₃ NO₂ Br OH 6463 OCH₂CH₂CH₃ OCH₂CH₂CH₃ NO₂ Br OH 6464 SCH₃ SCH₃ NO₂ Br OH 6465 SCH₂CH₃ SCH₂CH₃ NO₂ Br OH 6466 N(CH₃)₂ N(CH₃)₂ NO₂ Br OH 6467 N(CH₂CH₃)₂ N(CH₂CH₃)₂ NO₂ Br OH 6468 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) NO₂ Br OH 6469 O—(CH₂CH₂)—O NO₂ Br OH 6470 O—(CH₂CH₂CH₂)—O NO₂ Br OH 6471 S—(CH₂CH₂)—S NO₂ Br OH 6472 S—(CH₂CH₂CH₂)—S NO₂ Br OH 6473 —(CH₂)₄— NO₂ Br OH 6474 —(CH₂)₅— NO₂ Br OH 6475 H H CN Br OH 6476 CH₃ CH₃ CN Br OH 6477 CH₂CH₃ CH₂CH₃ CN Br OH 6478 CH₂CH₂CH₃ CH₂CH₂CH₃ CN Br OH 6479 OCH₃ OCH₃ CN Br OH 6480 OCH₂CH₃ OCH₂CH₃ CN Br OH 6481 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CN Br OH 6482 SCH₃ SCH₃ CN Br OH 6483 SCH₂CH₃ SCH₂CH₃ CN Br OH 6484 N(CH₃)₂ N(CH₃)₂ CN Br OH 6485 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CN Br OH 6486 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CN Br OH 6487 O—(CH₂CH₂)—O CN Br OH 6488 O—(CH₂CH₂CH₂)—O CN Br OH 6489 S—(CH₂CH₂)—S CN Br OH 6490 S—(CH₂CH₂CH₂)—S CN Br OH 6491 —(CH₂)₄— CN Br OH 6492 —(CH₂)₅— CN Br OH 6493 H H F Br OH 6494 CH₃ CH₃ F Br OH 6495 CH₂CH₃ CH₂CH₃ F Br OH 6496 CH₂CH₂CH₃ CH₂CH₂CH₃ F Br OH 6497 OCH₃ OCH₃ F Br OH 6498 OCH₂CH₃ OCH₂CH₃ F Br OH 6499 OCH₂CH₂CH₃ OCH₂CH₂CH₃ F Br OH 6500 SCH₃ SCH₃ F Br OH 6501 SCH₂CH₃ SCH₂CH₃ F Br OH 6502 N(CH₃)₂ N(CH₃)₂ F Br OH 6503 N(CH₂CH₃)₂ N(CH₂CH₃)₂ F Br OH 6504 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) F Br OH 6505 O—(CH₂CH₂)—O F Br OH 6506 O—(CH₂CH₂CH₂)—O F Br OH 6507 S—(CH₂CH₂)—S F Br OH 6508 S—(CH₂CH₂CH₂)—S F Br OH 6509 —(CH₂)₄— F Br OH 6510 —(CH₂)₅— F Br OH 6511 H H Cl Br OH 6512 CH₃ CH₃ Cl Br OH 6513 CH₂CH₃ CH₂CH₃ Cl Br OH 6514 CH₂CH₂CH₃ CH₂CH₂CH₃ Cl Br OH 6515 OCH₃ OCH₃ Cl Br OH 6516 OCH₂CH₃ OCH₂CH₃ Cl Br OH 6517 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Cl Br OH 6518 SCH₃ SCH₃ Cl Br OH 6519 SCH₂CH₃ SCH₂CH₃ Cl Br OH 6520 N(CH₃)₂ N(CH₃)₂ Cl Br OH 6521 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Cl Br OH 6522 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Cl Br OH 6523 O—(CH₂CH₂)—O Cl Br OH 6524 O—(CH₂CH₂CH₂)—O Cl Br OH 6525 S—(CH₂CH₂)—S Cl Br OH 6526 S—(CH₂CH₂CH₂)—S Cl Br OH 6527 —(CH₂)₄— Cl Br OH 6528 —(CH₂)₅— Cl Br OH 6529 H H Br Br OH 6530 CH₃ CH₃ Br Br OH 6531 CH₂CH₃ CH₂CH₃ Br Br OH 6532 CH₂CH₂CH₃ CH₂CH₂CH₃ Br Br OH 6533 OCH₃ OCH₃ Br Br OH 6534 OCH₂CH₃ OCH₂CH₃ Br Br OH 6535 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Br Br OH 6536 SCH₃ SCH₃ Br Br OH 6537 SCH₂CH₃ SCH₂CH₃ Br Br OH 6538 N(CH₃)₂ N(CH₃)₂ Br Br OH 6539 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Br Br OH 6540 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Br Br OH 6541 O—(CH₂CH₂)—O Br Br OH 6542 O—(CH₂CH₂CH₂)—O Br Br OH 6543 S—(CH₂CH₂)—S Br Br OH 6544 S—(CH₂CH₂CH₂)—S Br Br OH 6545 —(CH₂)₄— Br Br OH 6546 —(CH₂)₅— Br Br OH 6547 H H CH₃ Br OH 6548 CH₃ CH₃ CH₃ Br OH 6549 CH₂CH₃ CH₂CH₃ CH₃ Br OH 6550 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₃ Br OH 6551 OCH₃ OCH₃ CH₃ Br OH 6552 OCH₂CH₃ OCH₂CH₃ CH₃ Br OH 6553 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₃ Br OH 6554 SCH₃ SCH₃ CH₃ Br OH 6555 SCH₂CH₃ SCH₂CH₃ CH₃ Br OH 6556 N(CH₃)₂ N(CH₃)₂ CH₃ Br OH 6557 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₃ Br OH 6558 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₃ Br OH 6559 O—(CH₂CH₂)—O CH₃ Br OH 6560 O—(CH₂CH₂CH₂)—O CH₃ Br OH 6561 S—(CH₂CH₂)—S CH₃ Br OH 6562 S—(CH₂CH₂CH₂)—S CH₃ Br OH 6563 —(CH₂)₄— CH₃ Br OH 6564 —(CH₂)₅— CH₃ Br OH 6565 H H CH₂CH₃ Br OH 6566 CH₃ CH₃ CH₂CH₃ Br OH 6567 CH₂CH₃ CH₂CH₃ CH₂CH₃ Br OH 6568 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₂CH₃ Br OH 6569 OCH₃ OCH₃ CH₂CH₃ Br OH 6570 OCH₂CH₃ OCH₂CH₃ CH₂CH₃ Br OH 6571 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₂CH₃ Br OH 6572 SCH₃ SCH₃ CH₂CH₃ Br OH 6573 SCH₂CH₃ SCH₂CH₃ CH₂CH₃ Br OH 6574 N(CH₃)₂ N(CH₃)₂ CH₂CH₃ Br OH 6575 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₂CH₃ Br OH 6576 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₂CH₃ Br OH 6577 O—(CH₂CH₂)—O CH₂CH₃ Br OH 6578 O—(CH₂CH₂CH₂)—O CH₂CH₃ Br OH 6579 S—(CH₂CH₂)—S CH₂CH₃ Br OH 6580 S—(CH₂CH₂CH₂)—S CH₂CH₃ Br OH 6581 —(CH₂)₄— CH₂CH₃ Br OH 6582 —(CH₂)₅— CH₂CH₃ Br OH 6583 H H CF₃ Br OH 6584 CH₃ CH₃ CF₃ Br OH 6585 CH₂CH₃ CH₂CH₃ CF₃ Br OH 6586 CH₂CH₂CH₃ CH₂CH₂CH₃ CF₃ Br OH 6587 OCH₃ OCH₃ CF₃ Br OH 6588 OCH₂CH₃ OCH₂CH₃ CF₃ Br OH 6589 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CF₃ Br OH 6590 SCH₃ SCH₃ CF₃ Br OH 6591 SCH₂CH₃ SCH₂CH₃ CF₃ Br OH 6592 N(CH₃)₂ N(CH₃)₂ CF₃ Br OH 6593 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CF₃ Br OH 6594 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CF₃ Br OH 6595 O—(CH₂CH₂)—O CF₃ Br OH 6596 O—(CH₂CH₂CH₂)—O CF₃ Br OH 6597 S—(CH₂CH₂)—S CF₃ Br OH 6598 S—(CH₂CH₂CH₂)—S CF₃ Br OH 6599 —(CH₂)₄— CF₃ Br OH 6600 —(CH₂)₅— CF₃ Br OH 6601 H H OCH₃ Br OH 6602 CH₃ CH₃ OCH₃ Br OH 6603 CH₂CH₃ CH₂CH₃ OCH₃ Br OH 6604 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₃ Br OH 6605 OCH₃ OCH₃ OCH₃ Br OH 6606 OCH₂CH₃ OCH₂CH₃ OCH₃ Br OH 6607 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₃ Br OH 6608 SCH₃ SCH₃ OCH₃ Br OH 6609 SCH₂CH₃ SCH₂CH₃ OCH₃ Br OH 6610 N(CH₃)₂ N(CH₃)₂ OCH₃ Br OH 6611 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₃ Br OH 6612 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₃ Br OH 6613 O—(CH₂CH₂)—O OCH₃ Br OH 6614 O—(CH₂CH₂CH₂)—O OCH₃ Br OH 6615 S—(CH₂CH₂)—S OCH₃ Br OH 6616 S—(CH₂CH₂CH₂)—S OCH₃ Br OH 6617 —(CH₂)₄— OCH₃ Br OH 6618 —(CH₂)₅— OCH₃ Br OH 6619 H H OCH₂CH₃ Br OH 6620 CH₃ CH₃ OCH₂CH₃ Br OH 6621 CH₂CH₃ CH₂CH₃ OCH₂CH₃ Br OH 6622 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₂CH₃ Br OH 6623 OCH₃ OCH₃ OCH₂CH₃ Br OH 6624 OCH₂CH₃ OCH₂CH₃ OCH₂CH₃ Br OH 6625 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₂CH₃ Br OH 6626 SCH₃ SCH₃ OCH₂CH₃ Br OH 6627 SCH₂CH₃ SCH₂CH₃ OCH₂CH₃ Br OH 6628 N(CH₃)₂ N(CH₃)₂ OCH₂CH₃ Br OH 6629 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₂CH₃ Br OH 6630 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₂CH₃ Br OH 6631 O—(CH₂CH₂)—O OCH₂CH₃ Br OH 6632 O—(CH₂CH₂CH₂)—O OCH₂CH₃ Br OH 6633 S—(CH₂CH₂)—S OCH₂CH₃ Br OH 6634 S—(CH₂CH₂CH₂)—S OCH₂CH₃ Br OH 6635 —(CH₂)₄— OCH₂CH₃ Br OH 6636 —(CH₂)₅— OCH₂CH₃ Br OH 6637 H H SCH₃ Br OH 6638 CH₃ CH₃ SCH₃ Br OH 6639 CH₂CH₃ CH₂CH₃ SCH₃ Br OH 6640 CH₂CH₂CH₃ CH₂CH₂CH₃ SCH₃ Br OH 6641 OCH₃ OCH₃ SCH₃ Br OH 6642 OCH₂CH₃ OCH₂CH₃ SCH₃ Br OH 6643 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SCH₃ Br OH 6644 SCH₃ SCH₃ SCH₃ Br OH 6645 SCH₂CH₃ SCH₂CH₃ SCH₃ Br OH 6646 N(CH₃)₂ N(CH₃)₂ SCH₃ Br OH 6647 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SCH₃ Br OH 6648 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SCH₃ Br OH 6649 O—(CH₂CH₂)—O SCH₃ Br OH 6650 O—(CH₂CH₂CH₂)—O SCH₃ Br OH 6651 S—(CH₂CH₂)—S SCH₃ Br OH 6652 S—(CH₂CH₂CH₂)—S SCH₃ Br OH 6653 —(CH₂)₄— SCH₃ Br OH 6654 —(CH₂)₅— SCH₃ Br OH 6655 H H SO₂CH₃ Br OH 6656 CH₃ CH₃ SO₂CH₃ Br OH 6657 CH₂CH₃ CH₂CH₃ SO₂CH₃ Br OH 6658 CH₂CH₂CH₃ CH₂CH₂CH₃ SO₂CH₃ Br OH 6659 OCH₃ OCH₃ SO₂CH₃ Br OH 6660 OCH₂CH₃ OCH₂CH₃ SO₂CH₃ Br OH 6661 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SO₂CH₃ Br OH 6662 SCH₃ SCH₃ SO₂CH₃ Br OH 6663 SCH₂CH₃ SCH₂CH₃ SO₂CH₃ Br OH 6664 N(CH₃)₂ N(CH₃)₂ SO₂CH₃ Br OH 6665 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SO₂CH₃ Br OH 6666 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SO₂CH₃ Br OH 6667 O—(CH₂CH₂)—O SO₂CH₃ Br OH 6668 O—(CH₂CH₂CH₂)—O SO₂CH₃ Br OH 6669 S—(CH₂CH₂)—S SO₂CH₃ Br OH 6670 S—(CH₂CH₂CH₂)—S SO₂CH₃ Br OH 6671 —(CH₂)₄— SO₂CH₃ Br OH 6672 —(CH₂)₅— SO₂CH₃ Br OH 6673 H H PO(OCH₃)₂ Br OH 6674 CH₃ CH₃ PO(OCH₃)₂ Br OH 6675 CH₂CH₃ CH₂CH₃ PO(OCH₃)₂ Br OH 6676 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₃)₂ Br OH 6677 OCH₃ OCH₃ PO(OCH₃)₂ Br OH 6678 OCH₂CH₃ OCH₂CH₃ PO(OCH₃)₂ Br OH 6679 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₃)₂ Br OH 6680 SCH₃ SCH₃ PO(OCH₃)₂ Br OH 6681 SCH₂CH₃ SCH₂CH₃ PO(OCH₃)₂ Br OH 6682 N(CH₃)₂ N(CH₃)₂ PO(OCH₃)₂ Br OH 6683 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₃)₂ Br OH 6684 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₃)₂ Br OH 6685 O—(CH₂CH₂)—O PO(OCH₃)₂ Br OH 6686 O—(CH₂CH₂CH₂)—O PO(OCH₃)₂ Br OH 6687 S—(CH₂CH₂)—S PO(OCH₃)₂ Br OH 6688 S—(CH₂CH₂CH₂)—S PO(OCH₃)₂ Br OH 6689 —(CH₂)₄— PO(OCH₃)₂ Br OH 6690 —(CH₂)₅— PO(OCH₃)₂ Br OH 6691 H H PO(OCH₂CH₃)₂ Br OH 6692 CH₃ CH₃ PO(OCH₂CH₃)₂ Br OH 6693 CH₂CH₃ CH₂CH₃ PO(OCH₂CH₃)₂ Br OH 6694 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₂CH₃)₂ Br OH 6695 OCH₃ OCH₃ PO(OCH₂CH₃)₂ Br OH 6696 OCH₂CH₃ OCH₂CH₃ PO(OCH₂CH₃)₂ Br OH 6697 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₂CH₃)₂ Br OH 6698 SCH₃ SCH₃ PO(OCH₂CH₃)₂ Br OH 6699 SCH₂CH₃ SCH₂CH₃ PO(OCH₂CH₃)₂ Br OH 6700 N(CH₃)₂ N(CH₃)₂ PO(OCH₂CH₃)₂ Br OH 6701 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₂CH₃)₂ Br OH 6702 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₂CH₃)₂ Br OH 6703 O—(CH₂CH₂)—O PO(OCH₂CH₃)₂ Br OH 6704 O—(CH₂CH₂CH₂)—O PO(OCH₂CH₃)₂ Br OH 6705 S—(CH₂CH₂)—S PO(OCH₂CH₃)₂ Br OH 6706 S—(CH₂CH₂CH₂)—S PO(OCH₂CH₃)₂ Br OH 6707 —(CH₂)₄— PO(OCH₂CH₃)₂ Br OH 6708 —(CH₂)₅— PO(OCH₂CH₃)₂ Br OH 6709 H H PO(CH₃)₂ Br OH 6710 CH₃ CH₃ PO(CH₃)₂ Br OH 6711 CH₂CH₃ CH₂CH₃ PO(CH₃)₂ Br OH 6712 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₃)₂ Br OH 6713 OCH₃ OCH₃ PO(CH₃)₂ Br OH 6714 OCH₂CH₃ OCH₂CH₃ PO(CH₃)₂ Br OH 6715 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₃)₂ Br OH 6716 SCH₃ SCH₃ PO(CH₃)₂ Br OH 6717 SCH₂CH₃ SCH₂CH₃ PO(CH₃)₂ Br OH 6718 N(CH₃)₂ N(CH₃)₂ PO(CH₃)₂ Br OH 6719 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₃)₂ Br OH 6720 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₃)₂ Br OH 6721 O—(CH₂CH₂)—O PO(CH₃)₂ Br OH 6722 O—(CH₂CH₂CH₂)—O PO(CH₃)₂ Br OH 6723 S—(CH₂CH₂)—S PO(CH₃)₂ Br OH 6724 S—(CH₂CH₂CH₂)—S PO(CH₃)₂ Br OH 6725 —(CH₂)₄— PO(CH₃)₂ Br OH 6726 —(CH₂)₅— PO(CH₃)₂ Br OH 6727 H H PC(CH₂CH₃)₂ Br OH 6728 CH₃ CH₃ PC(CH₂CH₃)₂ Br OH 6729 CH₂CH₃ CH₂CH₃ PC(CH₂CH₃)₂ Br OH 6730 CH₂CH₂CH₃ CH₂CH₂CH₃ PC(CH₂CH₃)₂ Br OH 6731 OCH₃ OCH₃ PC(CH₂CH₃)₂ Br OH 6732 OCH₂CH₃ OCH₂CH₃ PC(CH₂CH₃)₂ Br OH 6733 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PC(CH₂CH₃)₂ Br OH 6734 SCH₃ SCH₃ PC(CH₂CH₃)₂ Br OH 6735 SCH₂CH₃ SCH₂CH₃ PC(CH₂CH₃)₂ Br OH 6736 N(CH₃)₂ N(CH₃)₂ PC(CH₂CH₃)₂ Br OH 6737 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PC(CH₂CH₃)₂ Br OH 6738 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PC(CH₂CH₃)₂ Br OH 6739 O—(CH₂CH₂)—O PC(CH₂CH₃)₂ Br OH 6740 O—(CH₂CH₂CH₂)—O PC(CH₂CH₃)₂ Br OH 6741 S—(CH₂CH₂)—S PC(CH₂CH₃)₂ Br OH 6742 S—(CH₂CH₂CH₂)—S PC(CH₂CH₃)₂ Br OH 6743 —(CH₂)₄— PC(CH₂CH₃)₂ Br OH 6744 —(CH₂)₅— PC(CH₂CH₃)₂ Br OH 6745 H H H Br OCOC₆H₅ 6746 CH₃ CH₃ H Br OCOC₆H₅ 6747 CH₂CH₃ CH₂CH₃ H Br OCOC₆H₅ 6748 CH₂CH₂CH₃ CH₂CH₂CH₃ H Br OCOC₆H₅ 6749 OCH₃ OCH₃ H Br OCOC₆H₅ 6750 OCH₂CH₃ OCH₂CH₃ H Br OCOC₆H₅ 6751 OCH₂CH₂CH₃ OCH₂CH₂CH₃ H Br OCOC₆H₅ 6752 SCH₃ SCH₃ H Br OCOC₆H₅ 6753 SCH₂CH₃ SCH₂CH₃ H Br OCOC₆H₅ 6754 N(CH₃)₂ N(CH₃)₂ H Br OCOC₆H₅ 6755 N(CH₂CH₃)₂ N(CH₂CH₃)₂ H Br OCOC₆H₅ 6756 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) H Br OCOC₆H₅ 6757 O—(CH₂CH₂)—O H Br OCOC₆H₅ 6758 O—(CH₂CH₂CH₂)—O H Br OCOC₆H₅ 6759 S—(CH₂CH₂)—S H Br OCOC₆H₅ 6760 S—(CH₂CH₂CH₂)—S H Br OCOC₆H₅ 6761 —(CH₂)₄— H Br OCOC₆H₅ 6762 —(CH₂)₅— H Br OCOC₆H₅ 6763 H H NO₂ Br OCOC₆H₅ 6764 CH₃ CH₃ NO₂ Br OCOC₆H₅ 6765 CH₂CH₃ CH₂CH₃ NO₂ Br OCOC₆H₅ 6766 CH₂CH₂CH₃ CH₂CH₂CH₃ NO₂ Br OCOC₆H₅ 6767 OCH₃ OCH₃ NO₂ Br OCOC₆H₅ 6768 OCH₂CH₃ OCH₂CH₃ NO₂ Br OCOC₆H₅ 6769 OCH₂CH₂CH₃ OCH₂CH₂CH₃ NO₂ Br OCOC₆H₅ 6770 SCH₃ SCH₃ NO₂ Br OCOC₆H₅ 6771 SCH₂CH₃ SCH₂CH₃ NO₂ Br OCOC₆H₅ 6772 N(CH₃)₂ N(CH₃)₂ NO₂ Br OCOC₆H₅ 6773 N(CH₂CH₃)₂ N(CH₂CH₃)₂ NO₂ Br OCOC₆H₅ 6774 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) NO₂ Br OCOC₆H₅ 6775 O—(CH₂CH₂)—O NO₂ Br OCOC₆H₅ 6776 O—(CH₂CH₂CH₂)—O NO₂ Br OCOC₆H₅ 6777 S—(CH₂CH₂)—S NO₂ Br OCOC₆H₅ 6778 S—(CH₂CH₂CH₂)—S NO₂ Br OCOC₆H₅ 6779 —(CH₂)₄— NO₂ Br OCOC₆H₅ 6780 —(CH₂)₅— NO₂ Br OCOC₆H₅ 6781 H H CN Br OCOC₆H₅ 6782 CH₃ CH₃ CN Br OCOC₆H₅ 6783 CH₂CH₃ CH₂CH₃ CN Br OCOC₆H₅ 6784 CH₂CH₂CH₃ CH₂CH₂CH₃ CN Br OCOC₆H₅ 6785 OCH₃ OCH₃ CN Br OCOC₆H₅ 6786 OCH₂CH₃ OCH₂CH₃ CN Br OCOC₆H₅ 6787 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CN Br OCOC₆H₅ 6788 SCH₃ SCH₃ CN Br OCOC₆H₅ 6789 SCH₂CH₃ SCH₂CH₃ CN Br OCOC₆H₅ 6790 N(CH₃)₂ N(CH₃)₂ CN Br OCOC₆H₅ 6791 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CN Br OCOC₆H₅ 6792 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CN Br OCOC₆H₅ 6793 O—(CH₂CH₂)—O CN Br OCOC₆H₅ 6794 O—(CH₂CH₂CH₂)—O CN Br OCOC₆H₅ 6795 S—(CH₂CH₂)—S CN Br OCOC₆H₅ 6796 S—(CH₂CH₂CH₂)—S CN Br OCOC₆H₅ 6797 —(CH₂)₄— CN Br OCOC₆H₅ 6798 —(CH₂)₅— CN Br OCOC₆H₅ 6799 H H F Br OCOC₆H₅ 6800 CH₃ CH₃ F Br OCOC₆H₅ 6801 CH₂CH₃ CH₂CH₃ F Br OCOC₆H₅ 6802 CH₂CH₂CH₃ CH₂CH₂CH₃ F Br OCOC₆H₅ 6803 OCH₃ OCH₃ F Br OCOC₆H₅ 6804 OCH₂CH₃ OCH₂CH₃ F Br OCOC₆H₅ 6805 OCH₂CH₂CH₃ OCH₂CH₂CH₃ F Br OCOC₆H₅ 6806 SCH₃ SCH₃ F Br OCOC₆H₅ 6807 SCH₂CH₃ SCH₂CH₃ F Br OCOC₆H₅ 6808 N(CH₃)₂ N(CH₃)₂ F Br OCOC₆H₅ 6809 N(CH₂CH₃)₂ N(CH₂CH₃)₂ F Br OCOC₆H₅ 6810 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) F Br OCOC₆H₅ 6811 O—(CH₂CH₂)—O F Br OCOC₆H₅ 6812 O—(CH₂CH₂CH₂)—O F Br OCOC₆H₅ 6813 S—(CH₂CH₂)—S F Br OCOC₆H₅ 6814 S—(CH₂CH₂CH₂)—S F Br OCOC₆H₅ 6815 —(CH₂)₄— F Br OCOC₆H₅ 6816 —(CH₂)₅— F Br OCOC₆H₅ 6817 H H Cl Br OCOC₆H₅ 6818 CH₃ CH₃ Cl Br OCOC₆H₅ 6819 CH₂CH₃ CH₂CH₃ Cl Br OCOC₆H₅ 6820 CH₂CH₂CH₃ CH₂CH₂CH₃ Cl Br OCOC₆H₅ 6821 OCH₃ OCH₃ Cl Br OCOC₆H₅ 6822 OCH₂CH₃ OCH₂CH₃ Cl Br OCOC₆H₅ 6823 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Cl Br OCOC₆H₅ 6824 SCH₃ SCH₃ Cl Br OCOC₆H₅ 6825 SCH₂CH₃ SCH₂CH₃ Cl Br OCOC₆H₅ 6826 N(CH₃)₂ N(CH₃)₂ Cl Br OCOC₆H₅ 6827 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Cl Br OCOC₆H₅ 6828 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Cl Br OCOC₆H₅ 6829 O—(CH₂CH₂)—O Cl Br OCOC₆H₅ 6830 O—(CH₂CH₂CH₂)—O Cl Br OCOC₆H₅ 6831 S—(CH₂CH₂)—S Cl Br OCOC₆H₅ 6832 S—(CH₂CH₂CH₂)—S Cl Br OCOC₆H₅ 6833 —(CH₂)₄— Cl Br OCOC₆H₅ 6834 —(CH₂)₅— Cl Br OCOC₆H₅ 6835 H H Br Br OCOC₆H₅ 6836 CH₃ CH₃ Br Br OCOC₆H₅ 6837 CH₂CH₃ CH₂CH₃ Br Br OCOC₆H₅ 6838 CH₂CH₂CH₃ CH₂CH₂CH₃ Br Br OCOC₆H₅ 6839 OCH₃ OCH₃ Br Br OCOC₆H₅ 6840 OCH₂CH₃ OCH₂CH₃ Br Br OCOC₆H₅ 6841 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Br Br OCOC₆H₅ 6842 SCH₃ SCH₃ Br Br OCOC₆H₅ 6843 SCH₂CH₃ SCH₂CH₃ Br Br OCOC₆H₅ 6844 N(CH₃)₂ N(CH₃)₂ Br Br OCOC₆H₅ 6845 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Br Br OCOC₆H₅ 6846 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Br Br OCOC₆H₅ 6847 O—(CH₂CH₂)—O Br Br OCOC₆H₅ 6848 O—(CH₂CH₂CH₂)—O Br Br OCOC₆H₅ 6849 S—(CH₂CH₂)—S Br Br OCOC₆H₅ 6850 S—(CH₂CH₂CH₂)—S Br Br OCOC₆H₅ 6851 —(CH₂)₄— Br Br OCOC₆H₅ 6852 —(CH₂)₅— Br Br OCOC₆H₅ 6853 H H CH₃ Br OCOC₆H₅ 6854 CH₃ CH₃ CH₃ Br OCOC₆H₅ 6855 CH₂CH₃ CH₂CH₃ CH₃ Br OCOC₆H₅ 6856 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₃ Br OCOC₆H₅ 6857 OCH₃ OCH₃ CH₃ Br OCOC₆H₅ 6858 OCH₂CH₃ OCH₂CH₃ CH₃ Br OCOC₆H₅ 6859 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₃ Br OCOC₆H₅ 6860 SCH₃ SCH₃ CH₃ Br OCOC₆H₅ 6861 SCH₂CH₃ SCH₂CH₃ CH₃ Br OCOC₆H₅ 6862 N(CH₃)₂ N(CH₃)₂ CH₃ Br OCOC₆H₅ 6863 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₃ Br OCOC₆H₅ 6864 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₃ Br OCOC₆H₅ 6865 O—(CH₂CH₂)—O CH₃ Br OCOC₆H₅ 6866 O—(CH₂CH₂CH₂)—O CH₃ Br OCOC₆H₅ 6867 S—(CH₂CH₂)—S CH₃ Br OCOC₆H₅ 6868 S—(CH₂CH₂CH₂)—S CH₃ Br OCOC₆H₅ 6869 —(CH₂)₄— CH₃ Br OCOC₆H₅ 6870 —(CH₂)₅— CH₃ Br OCOC₆H₅ 6871 H H CH₂CH₃ Br OCOC₆H₅ 6872 CH₃ CH₃ CH₂CH₃ Br OCOC₆H₅ 6873 CH₂CH₃ CH₂CH₃ CH₂CH₃ Br OCOC₆H₅ 6874 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₂CH₃ Br OCOC₆H₅ 6875 OCH₃ OCH₃ CH₂CH₃ Br OCOC₆H₅ 6876 OCH₂CH₃ OCH₂CH₃ CH₂CH₃ Br OCOC₆H₅ 6877 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₂CH₃ Br OCOC₆H₅ 6878 SCH₃ SCH₃ CH₂CH₃ Br OCOC₆H₅ 6879 SCH₂CH₃ SCH₂CH₃ CH₂CH₃ Br OCOC₆H₅ 6880 N(CH₃)₂ N(CH₃)₂ CH₂CH₃ Br OCOC₆H₅ 6881 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₂CH₃ Br OCOC₆H₅ 6882 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₂CH₃ Br OCOC₆H₅ 6883 O—(CH₂CH₂)—O CH₂CH₃ Br OCOC₆H₅ 6884 O—(CH₂CH₂CH₂)—O CH₂CH₃ Br OCOC₆H₅ 6885 S—(CH₂CH₂)—S CH₂CH₃ Br OCOC₆H₅ 6886 S—(CH₂CH₂CH₂)—S CH₂CH₃ Br OCOC₆H₅ 6887 —(CH₂)₄— CH₂CH₃ Br OCOC₆H₅ 6888 —(CH₂)₅— CH₂CH₃ Br OCOC₆H₅ 6889 H H CF₃ Br OCOC₆H₅ 6890 CH₃ CH₃ CF₃ Br OCOC₆H₅ 6891 CH₂CH₃ CH₂CH₃ CF₃ Br OCOC₆H₅ 6892 CH₂CH₂CH₃ CH₂CH₂CH₃ CF₃ Br OCOC₆H₅ 6893 OCH₃ OCH₃ CF₃ Br OCOC₆H₅ 6894 OCH₂CH₃ OCH₂CH₃ CF₃ Br OCOC₆H₅ 6895 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CF₃ Br OCOC₆H₅ 6896 SCH₃ SCH₃ CF₃ Br OCOC₆H₅ 6897 SCH₂CH₃ SCH₂CH₃ CF₃ Br OCOC₆H₅ 6898 N(CH₃)₂ N(CH₃)₂ CF₃ Br OCOC₆H₅ 6899 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CF₃ Br OCOC₆H₅ 6900 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CF₃ Br OCOC₆H₅ 6901 O—(CH₂CH₂)—O CF₃ Br OCOC₆H₅ 6902 O—(CH₂CH₂CH₂)—O CF₃ Br OCOC₆H₅ 6903 S—(CH₂CH₂)—S CF₃ Br OCOC₆H₅ 6904 S—(CH₂CH₂CH₂)—S CF₃ Br OCOC₆H₅ 6905 —(CH₂)₄— CF₃ Br OCOC₆H₅ 6906 —(CH₂)₅— CF₃ Br OCOC₆H₅ 6907 H H OCH₃ Br OCOC₆H₅ 6908 CH₃ CH₃ OCH₃ Br OCOC₆H₅ 6909 CH₂CH₃ CH₂CH₃ OCH₃ Br OCOC₆H₅ 6910 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₃ Br OCOC₆H₅ 6911 OCH₃ OCH₃ OCH₃ Br OCOC₆H₅ 6912 OCH₂CH₃ OCH₂CH₃ OCH₃ Br OCOC₆H₅ 6913 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₃ Br OCOC₆H₅ 6914 SCH₃ SCH₃ OCH₃ Br OCOC₆H₅ 6915 SCH₂CH₃ SCH₂CH₃ OCH₃ Br OCOC₆H₅ 6916 N(CH₃)₂ N(CH₃)₂ OCH₃ Br OCOC₆H₅ 6917 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₃ Br OCOC₆H₅ 6918 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₃ Br OCOC₆H₅ 6919 O—(CH₂CH₂)—O OCH₃ Br OCOC₆H₅ 6920 O—(CH₂CH₂CH₂)—O OCH₃ Br OCOC₆H₅ 6921 S—(CH₂CH₂)—S OCH₃ Br OCOC₆H₅ 6922 S—(CH₂CH₂CH₂)—S OCH₃ Br OCOC₆H₅ 6923 —(CH₂)₄— OCH₃ Br OCOC₆H₅ 6924 —(CH₂)₅— OCH₃ Br OCOC₆H₅ 6925 H H OCH₂CH₃ Br OCOC₆H₅ 6926 CH₃ CH₃ OCH₂CH₃ Br OCOC₆H₅ 6927 CH₂CH₃ CH₂CH₃ OCH₂CH₃ Br OCOC₆H₅ 6928 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₂CH₃ Br OCOC₆H₅ 6929 OCH₃ OCH₃ OCH₂CH₃ Br OCOC₆H₅ 6930 OCH₂CH₃ OCH₂CH₃ OCH₂CH₃ Br OCOC₆H₅ 6931 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₂CH₃ Br OCOC₆H₅ 6932 SCH₃ SCH₃ OCH₂CH₃ Br OCOC₆H₅ 6933 SCH₂CH₃ SCH₂CH₃ OCH₂CH₃ Br OCOC₆H₅ 6934 N(CH₃)₂ N(CH₃)₂ OCH₂CH₃ Br OCOC₆H₅ 6935 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₂CH₃ Br OCOC₆H₅ 6936 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₂CH₃ Br OCOC₆H₅ 6937 O—(CH₂CH₂)—O OCH₂CH₃ Br OCOC₆H₅ 6938 O—(CH₂CH₂CH₂)—O OCH₂CH₃ Br OCOC₆H₅ 6939 S—(CH₂CH₂)—S OCH₂CH₃ Br OCOC₆H₅ 6940 S—(CH₂CH₂CH₂)—S OCH₂CH₃ Br OCOC₆H₅ 6941 —(CH₂)₄— OCH₂CH₃ Br OCOC₆H₅ 6942 —(CH₂)₅— OCH₂CH₃ Br OCOC₆H₅ 6943 H H SCH₃ Br OCOC₆H₅ 6944 CH₃ CH₃ SCH₃ Br OCOC₆H₅ 6945 CH₂CH₃ CH₂CH₃ SCH₃ Br OCOC₆H₅ 6946 CH₂CH₂CH₃ CH₂CH₂CH₃ SCH₃ Br OCOC₆H₅ 6947 OCH₃ OCH₃ SCH₃ Br OCOC₆H₅ 6948 OCH₂CH₃ OCH₂CH₃ SCH₃ Br OCOC₆H₅ 6949 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SCH₃ Br OCOC₆H₅ 6950 SCH₃ SCH₃ SCH₃ Br OCOC₆H₅ 6951 SCH₂CH₃ SCH₂CH₃ SCH₃ Br OCOC₆H₅ 6952 N(CH₃)₂ N(CH₃)₂ SCH₃ Br OCOC₆H₅ 6953 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SCH₃ Br OCOC₆H₅ 6954 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SCH₃ Br OCOC₆H₅ 6955 O—(CH₂CH₂)—O SCH₃ Br OCOC₆H₅ 6956 O—(CH₂CH₂CH₂)—O SCH₃ Br OCOC₆H₅ 6957 S—(CH₂CH₂)—S SCH₃ Br OCOC₆H₅ 6958 S—(CH₂CH₂CH₂)—S SCH₃ Br OCOC₆H₅ 6959 —(CH₂)₄— SCH₃ Br OCOC₆H₅ 6960 —(CH₂)₅— SCH₃ Br OCOC₆H₅ 6961 H H SO₂CH₃ Br OCOC₆H₅ 6962 CH₃ CH₃ SO₂CH₃ Br OCOC₆H₅ 6963 CH₂CH₃ CH₂CH₃ SO₂CH₃ Br OCOC₆H₅ 6964 CH₂CH₂CH₃ CH₂CH₂CH₃ SO₂CH₃ Br OCOC₆H₅ 6965 OCH₃ OCH₃ SO₂CH₃ Br OCOC₆H₅ 6966 OCH₂CH₃ OCH₂CH₃ SO₂CH₃ Br OCOC₆H₅ 6967 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SO₂CH₃ Br OCOC₆H₅ 6968 SCH₃ SCH₃ SO₂CH₃ Br OCOC₆H₅ 6969 SCH₂CH₃ SCH₂CH₃ SO₂CH₃ Br OCOC₆H₅ 6970 N(CH₃)₂ N(CH₃)₂ SO₂CH₃ Br OCOC₆H₅ 6971 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SO₂CH₃ Br OCOC₆H₅ 6972 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SO₂CH₃ Br OCOC₆H₅ 6973 O—(CH₂CH₂)—O SO₂CH₃ Br OCOC₆H₅ 6974 O—(CH₂CH₂CH₂)—O SO₂CH₃ Br OCOC₆H₅ 6975 S—(CH₂CH₂)—S SO₂CH₃ Br OCOC₆H₅ 6976 S—(CH₂CH₂CH₂)—S SO₂CH₃ Br OCOC₆H₅ 6977 —(CH₂)₄— SO₂CH₃ Br OCOC₆H₅ 6978 —(CH₂)₅— SO₂CH₃ Br OCOC₆H₅ 6979 H H PO(OCH₃)₂ Br OCOC₆H₅ 6980 CH₃ CH₃ PO(OCH₃)₂ Br OCOC₆H₅ 6981 CH₂CH₃ CH₂CH₃ PO(OCH₃)₂ Br OCOC₆H₅ 6982 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₃)₂ Br OCOC₆H₅ 6983 OCH₃ OCH₃ PO(OCH₃)₂ Br OCOC₆H₅ 6984 OCH₂CH₃ OCH₂CH₃ PO(OCH₃)₂ Br OCOC₆H₅ 6985 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₃)₂ Br OCOC₆H₅ 6986 SCH₃ SCH₃ PO(OCH₃)₂ Br OCOC₆H₅ 6987 SCH₂CH₃ SCH₂CH₃ PO(OCH₃)₂ Br OCOC₆H₅ 6988 N(CH₃)₂ N(CH₃)₂ PO(OCH₃)₂ Br OCOC₆H₅ 6989 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₃)₂ Br OCOC₆H₅ 6990 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₃)₂ Br OCOC₆H₅ 6991 O—(CH₂CH₂)—O PO(OCH₃)₂ Br OCOC₆H₅ 6992 O—(CH₂CH₂CH₂)—O PO(OCH₃)₂ Br OCOC₆H₅ 6993 S—(CH₂CH₂)—S PO(OCH₃)₂ Br OCOC₆H₅ 6994 S—(CH₂CH₂CH₂)—S PO(OCH₃)₂ Br OCOC₆H₅ 6995 —(CH₂)₄— PO(OCH₃)₂ Br OCOC₆H₅ 6996 —(CH₂)₅— PO(OCH₃)₂ Br OCOC₆H₅ 6997 H H PO(OCH₂CH₃)₂ Br OCOC₆H₅ 6998 CH₃ CH₃ PO(OCH₂CH₃)₂ Br OCOC₆H₅ 6999 CH₂CH₃ CH₂CH₃ PO(OCH₂CH₃)₂ Br OCOC₆H₅ 7000 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₂CH₃)₂ Br OCOC₆H₅ 7001 OCH₃ OCH₃ PO(OCH₂CH₃)₂ Br OCOC₆H₅ 7002 OCH₂CH₃ OCH₂CH₃ PO(OCH₂CH₃)₂ Br OCOC₆H₅ 7003 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₂CH₃)₂ Br OCOC₆H₅ 7004 SCH₃ SCH₃ PO(OCH₂CH₃)₂ Br OCOC₆H₅ 7005 SCH₂CH₃ SCH₂CH₃ PO(OCH₂CH₃)₂ Br OCOC₆H₅ 7006 N(CH₃)₂ N(CH₃)₂ PO(OCH₂CH₃)₂ Br OCOC₆H₅ 7007 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₂CH₃)₂ Br OCOC₆H₅ 7008 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₂CH₃)₂ Br OCOC₆H₅ 7009 O—(CH₂CH₂)—O PO(OCH₂CH₃)₂ Br OCOC₆H₅ 7010 O—(CH₂CH₂CH₂)—O PO(OCH₂CH₃)₂ Br OCOC₆H₅ 7011 S—(CH₂CH₂)—S PO(OCH₂CH₃)₂ Br OCOC₆H₅ 7012 S—(CH₂CH₂CH₂)—S PO(OCH₂CH₃)₂ Br OCOC₆H₅ 7013 —(CH₂)₄— PO(OCH₂CH₃)₂ Br OCOC₆H₅ 7014 —(CH₂)₅— PO(OCH₂CH₃)₂ Br OCOC₆H₅ 7015 H H PO(CH₃)₂ Br OCOC₆H₅ 7016 CH₃ CH₃ PO(CH₃)₂ Br OCOC₆H₅ 7017 CH₂CH₃ CH₂CH₃ PO(CH₃)₂ Br OCOC₆H₅ 7018 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₃)₂ Br OCOC₆H₅ 7019 OCH₃ OCH₃ PO(CH₃)₂ Br OCOC₆H₅ 7020 OCH₂CH₃ OCH₂CH₃ PO(CH₃)₂ Br OCOC₆H₅ 7021 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₃)₂ Br OCOC₆H₅ 7022 SCH₃ SCH₃ PO(CH₃)₂ Br OCOC₆H₅ 7023 SCH₂CH₃ SCH₂CH₃ PO(CH₃)₂ Br OCOC₆H₅ 7024 N(CH₃)₂ N(CH₃)₂ PO(CH₃)₂ Br OCOC₆H₅ 7025 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₃)₂ Br OCOC₆H₅ 7026 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₃)₂ Br OCOC₆H₅ 7027 O—(CH₂CH₂)—O PO(CH₃)₂ Br OCOC₆H₅ 7028 O—(CH₂CH₂CH₂)—O PO(CH₃)₂ Br OCOC₆H₅ 7029 S—(CH₂CH₂)—S PO(CH₃)₂ Br OCOC₆H₅ 7030 S—(CH₂CH₂CH₂)—S PO(CH₃)₂ Br OCOC₆H₅ 7031 —(CH₂)₄— PO(CH₃)₂ Br OCOC₆H₅ 7032 —(CH₂)₅— PO(CH₃)₂ Br OCOC₆H₅ 7033 H H PC(CH₂CH₃)₂ Br OCOC₆H₅ 7034 CH₃ CH₃ PC(CH₂CH₃)₂ Br OCOC₆H₅ 7035 CH₂CH₃ CH₂CH₃ PC(CH₂CH₃)₂ Br OCOC₆H₅ 7036 CH₂CH₂CH₃ CH₂CH₂CH₃ PC(CH₂CH₃)₂ Br OCOC₆H₅ 7037 OCH₃ OCH₃ PC(CH₂CH₃)₂ Br OCOC₆H₅ 7038 OCH₂CH₃ OCH₂CH₃ PC(CH₂CH₃)₂ Br OCOC₆H₅ 7039 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PC(CH₂CH₃)₂ Br OCOC₆H₅ 7040 SCH₃ SCH₃ PC(CH₂CH₃)₂ Br OCOC₆H₅ 7041 SCH₂CH₃ SCH₂CH₃ PC(CH₂CH₃)₂ Br OCOC₆H₅ 7042 N(CH₃)₂ N(CH₃)₂ PC(CH₂CH₃)₂ Br OCOC₆H₅ 7043 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PC(CH₂CH₃)₂ Br OCOC₆H₅ 7044 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PC(CH₂CH₃)₂ Br OCOC₆H₅ 7045 O—(CH₂CH₂)—O PC(CH₂CH₃)₂ Br OCOC₆H₅ 7046 O—(CH₂CH₂CH₂)—O PC(CH₂CH₃)₂ Br OCOC₆H₅ 7047 S—(CH₂CH₂)—S PC(CH₂CH₃)₂ Br OCOC₆H₅ 7048 S—(CH₂CH₂CH₂)—S PC(CH₂CH₃)₂ Br OCOC₆H₅ 7049 —(CH₂)₄— PC(CH₂CH₃)₂ Br OCOC₆H₅ 7050 —(CH₂)₅— PC(CH₂CH₃)₂ Br OCOC₆H₅ 7051 H H H Br SCH₃ 7052 CH₃ CH₃ H Br SCH₃ 7053 CH₂CH₃ CH₂CH₃ H Br SCH₃ 7054 CH₂CH₂CH₃ CH₂CH₂CH₃ H Br SCH₃ 7055 OCH₃ OCH₃ H Br SCH₃ 7056 OCH₂CH₃ OCH₂CH₃ H Br SCH₃ 7057 OCH₂CH₂CH₃ OCH₂CH₂CH₃ H Br SCH₃ 7058 SCH₃ SCH₃ H Br SCH₃ 7059 SCH₂CH₃ SCH₂CH₃ H Br SCH₃ 7060 N(CH₃)₂ N(CH₃)₂ H Br SCH₃ 7061 N(CH₂CH₃)₂ N(CH₂CH₃)₂ H Br SCH₃ 7062 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) H Br SCH₃ 7063 O—(CH₂CH₂)—O H Br SCH₃ 7064 O—(CH₂CH₂CH₂)—O H Br SCH₃ 7065 S—(CH₂CH₂)—S H Br SCH₃ 7066 S—(CH₂CH₂CH₂)—S H Br SCH₃ 7067 —(CH₂)₄— H Br SCH₃ 7068 —(CH₂)₅— H Br SCH₃ 7069 H H NO₂ Br SCH₃ 7070 CH₃ CH₃ NO₂ Br SCH₃ 7071 CH₂CH₃ CH₂CH₃ NO₂ Br SCH₃ 7072 CH₂CH₂CH₃ CH₂CH₂CH₃ NO₂ Br SCH₃ 7073 OCH₃ OCH₃ NO₂ Br SCH₃ 7074 OCH₂CH₃ OCH₂CH₃ NO₂ Br SCH₃ 7075 OCH₂CH₂CH₃ OCH₂CH₂CH₃ NO₂ Br SCH₃ 7076 SCH₃ SCH₃ NO₂ Br SCH₃ 7077 SCH₂CH₃ SCH₂CH₃ NO₂ Br SCH₃ 7078 N(CH₃)₂ N(CH₃)₂ NO₂ Br SCH₃ 7079 N(CH₂CH₃)₂ N(CH₂CH₃)₂ NO₂ Br SCH₃ 7080 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) NO₂ Br SCH₃ 7081 O—(CH₂CH₂)—O NO₂ Br SCH₃ 7082 O—(CH₂CH₂CH₂)—O NO₂ Br SCH₃ 7083 S—(CH₂CH₂)—S NO₂ Br SCH₃ 7084 S—(CH₂CH₂CH₂)—S NO₂ Br SCH₃ 7085 —(CH₂)₄— NO₂ Br SCH₃ 7086 —(CH₂)₅— NO₂ Br SCH₃ 7087 H H CN Br SCH₃ 7088 CH₃ CH₃ CN Br SCH₃ 7089 CH₂CH₃ CH₂CH₃ CN Br SCH₃ 7090 CH₂CH₂CH₃ CH₂CH₂CH₃ CN Br SCH₃ 7091 OCH₃ OCH₃ CN Br SCH₃ 7092 OCH₂CH₃ OCH₂CH₃ CN Br SCH₃ 7093 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CN Br SCH₃ 7094 SCH₃ SCH₃ CN Br SCH₃ 7095 SCH₂CH₃ SCH₂CH₃ CN Br SCH₃ 7096 N(CH₃)₂ N(CH₃)₂ CN Br SCH₃ 7097 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CN Br SCH₃ 7098 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CN Br SCH₃ 7099 O—(CH₂CH₂)—O CN Br SCH₃ 7100 O—(CH₂CH₂CH₂)—O CN Br SCH₃ 7101 S—(CH₂CH₂)—S CN Br SCH₃ 7102 S—(CH₂CH₂CH₂)—S CN Br SCH₃ 7103 —(CH₂)₄— CN Br SCH₃ 7104 —(CH₂)₅— CN Br SCH₃ 7105 H H F Br SCH₃ 7106 CH₃ CH₃ F Br SCH₃ 7107 CH₂CH₃ CH₂CH₃ F Br SCH₃ 7108 CH₂CH₂CH₃ CH₂CH₂CH₃ F Br SCH₃ 7109 OCH₃ OCH₃ F Br SCH₃ 7110 OCH₂CH₃ OCH₂CH₃ F Br SCH₃ 7111 OCH₂CH₂CH₃ OCH₂CH₂CH₃ F Br SCH₃ 7112 SCH₃ SCH₃ F Br SCH₃ 7113 SCH₂CH₃ SCH₂CH₃ F Br SCH₃ 7114 N(CH₃)₂ N(CH₃)₂ F Br SCH₃ 7115 N(CH₂CH₃)₂ N(CH₂CH₃)₂ F Br SCH₃ 7116 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) F Br SCH₃ 7117 O—(CH₂CH₂)—O F Br SCH₃ 7118 O—(CH₂CH₂CH₂)—O F Br SCH₃ 7119 S—(CH₂CH₂)—S F Br SCH₃ 7120 S—(CH₂CH₂CH₂)—S F Br SCH₃ 7121 —(CH₂)₄— F Br SCH₃ 7122 —(CH₂)₅— F Br SCH₃ 7123 H H Cl Br SCH₃ 7124 CH₃ CH₃ Cl Br SCH₃ 7125 CH₂CH₃ CH₂CH₃ Cl Br SCH₃ 7126 CH₂CH₂CH₃ CH₂CH₂CH₃ Cl Br SCH₃ 7127 OCH₃ OCH₃ Cl Br SCH₃ 7128 OCH₂CH₃ OCH₂CH₃ Cl Br SCH₃ 7129 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Cl Br SCH₃ 7130 SCH₃ SCH₃ Cl Br SCH₃ 7131 SCH₂CH₃ SCH₂CH₃ Cl Br SCH₃ 7132 N(CH₃)₂ N(CH₃)₂ Cl Br SCH₃ 7133 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Cl Br SCH₃ 7134 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Cl Br SCH₃ 7135 O—(CH₂CH₂)—O Cl Br SCH₃ 7136 O—(CH₂CH₂CH₂)—O Cl Br SCH₃ 7137 S—(CH₂CH₂)—S Cl Br SCH₃ 7138 S—(CH₂CH₂CH₂)—S Cl Br SCH₃ 7139 —(CH₂)₄— Cl Br SCH₃ 7140 —(CH₂)₅— Cl Br SCH₃ 7141 H H Br Br SCH₃ 7142 CH₃ CH₃ Br Br SCH₃ 7143 CH₂CH₃ CH₂CH₃ Br Br SCH₃ 7144 CH₂CH₂CH₃ CH₂CH₂CH₃ Br Br SCH₃ 7145 OCH₃ OCH₃ Br Br SCH₃ 7146 OCH₂CH₃ OCH₂CH₃ Br Br SCH₃ 7147 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Br Br SCH₃ 7148 SCH₃ SCH₃ Br Br SCH₃ 7149 SCH₂CH₃ SCH₂CH₃ Br Br SCH₃ 7150 N(CH₃)₂ N(CH₃)₂ Br Br SCH₃ 7151 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Br Br SCH₃ 7152 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Br Br SCH₃ 7153 O—(CH₂CH₂)—O Br Br SCH₃ 7154 O—(CH₂CH₂CH₂)—O Br Br SCH₃ 7155 S—(CH₂CH₂)—S Br Br SCH₃ 7156 S—(CH₂CH₂CH₂)—S Br Br SCH₃ 7157 —(CH₂)₄— Br Br SCH₃ 7158 —(CH₂)₅— Br Br SCH₃ 7159 H H CH₃ Br SCH₃ 7160 CH₃ CH₃ CH₃ Br SCH₃ 7161 CH₂CH₃ CH₂CH₃ CH₃ Br SCH₃ 7162 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₃ Br SCH₃ 7163 OCH₃ OCH₃ CH₃ Br SCH₃ 7164 OCH₂CH₃ OCH₂CH₃ CH₃ Br SCH₃ 7165 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₃ Br SCH₃ 7166 SCH₃ SCH₃ CH₃ Br SCH₃ 7167 SCH₂CH₃ SCH₂CH₃ CH₃ Br SCH₃ 7168 N(CH₃)₂ N(CH₃)₂ CH₃ Br SCH₃ 7169 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₃ Br SCH₃ 7170 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₃ Br SCH₃ 7171 O—(CH₂CH₂)—O CH₃ Br SCH₃ 7172 O—(CH₂CH₂CH₂)—O CH₃ Br SCH₃ 7173 S—(CH₂CH₂)—S CH₃ Br SCH₃ 7174 S—(CH₂CH₂CH₂)—S CH₃ Br SCH₃ 7175 —(CH₂)₄— CH₃ Br SCH₃ 7176 —(CH₂)₅— CH₃ Br SCH₃ 7177 H H CH₂CH₃ Br SCH₃ 7178 CH₃ CH₃ CH₂CH₃ Br SCH₃ 7179 CH₂CH₃ CH₂CH₃ CH₂CH₃ Br SCH₃ 7180 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₂CH₃ Br SCH₃ 7181 OCH₃ OCH₃ CH₂CH₃ Br SCH₃ 7182 OCH₂CH₃ OCH₂CH₃ CH₂CH₃ Br SCH₃ 7183 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₂CH₃ Br SCH₃ 7184 SCH₃ SCH₃ CH₂CH₃ Br SCH₃ 7185 SCH₂CH₃ SCH₂CH₃ CH₂CH₃ Br SCH₃ 7186 N(CH₃)₂ N(CH₃)₂ CH₂CH₃ Br SCH₃ 7187 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₂CH₃ Br SCH₃ 7188 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₂CH₃ Br SCH₃ 7189 O—(CH₂CH₂)—O CH₂CH₃ Br SCH₃ 7190 O—(CH₂CH₂CH₂)—O CH₂CH₃ Br SCH₃ 7191 S—(CH₂CH₂)—S CH₂CH₃ Br SCH₃ 7192 S—(CH₂CH₂CH₂)—S CH₂CH₃ Br SCH₃ 7193 —(CH₂)₄— CH₂CH₃ Br SCH₃ 7194 —(CH₂)₅— CH₂CH₃ Br SCH₃ 7195 H H CF₃ Br SCH₃ 7196 CH₃ CH₃ CF₃ Br SCH₃ 7197 CH₂CH₃ CH₂CH₃ CF₃ Br SCH₃ 7198 CH₂CH₂CH₃ CH₂CH₂CH₃ CF₃ Br SCH₃ 7199 OCH₃ OCH₃ CF₃ Br SCH₃ 7200 OCH₂CH₃ OCH₂CH₃ CF₃ Br SCH₃ 7201 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CF₃ Br SCH₃ 7202 SCH₃ SCH₃ CF₃ Br SCH₃ 7203 SCH₂CH₃ SCH₂CH₃ CF₃ Br SCH₃ 7204 N(CH₃)₂ N(CH₃)₂ CF₃ Br SCH₃ 7205 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CF₃ Br SCH₃ 7206 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CF₃ Br SCH₃ 7207 O—(CH₂CH₂)—O CF₃ Br SCH₃ 7208 O—(CH₂CH₂CH₂)—O CF₃ Br SCH₃ 7209 S—(CH₂CH₂)—S CF₃ Br SCH₃ 7210 S—(CH₂CH₂CH₂)—S CF₃ Br SCH₃ 7211 —(CH₂)₄— CF₃ Br SCH₃ 7212 —(CH₂)₅— CF₃ Br SCH₃ 7213 H H OCH₃ Br SCH₃ 7214 CH₃ CH₃ OCH₃ Br SCH₃ 7215 CH₂CH₃ CH₂CH₃ OCH₃ Br SCH₃ 7216 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₃ Br SCH₃ 7217 OCH₃ OCH₃ OCH₃ Br SCH₃ 7218 OCH₂CH₃ OCH₂CH₃ OCH₃ Br SCH₃ 7219 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₃ Br SCH₃ 7220 SCH₃ SCH₃ OCH₃ Br SCH₃ 7221 SCH₂CH₃ SCH₂CH₃ OCH₃ Br SCH₃ 7222 N(CH₃)₂ N(CH₃)₂ OCH₃ Br SCH₃ 7223 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₃ Br SCH₃ 7224 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₃ Br SCH₃ 7225 O—(CH₂CH₂)—O OCH₃ Br SCH₃ 7226 O—(CH₂CH₂CH₂)—O OCH₃ Br SCH₃ 7227 S—(CH₂CH₂)—S OCH₃ Br SCH₃ 7228 S—(CH₂CH₂CH₂)—S OCH₃ Br SCH₃ 7229 —(CH₂)₄— OCH₃ Br SCH₃ 7230 —(CH₂)₅— OCH₃ Br SCH₃ 7231 H H OCH₂CH₃ Br SCH₃ 7232 CH₃ CH₃ OCH₂CH₃ Br SCH₃ 7233 CH₂CH₃ CH₂CH₃ OCH₂CH₃ Br SCH₃ 7234 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₂CH₃ Br SCH₃ 7235 OCH₃ OCH₃ OCH₂CH₃ Br SCH₃ 7236 OCH₂CH₃ OCH₂CH₃ OCH₂CH₃ Br SCH₃ 7237 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₂CH₃ Br SCH₃ 7238 SCH₃ SCH₃ OCH₂CH₃ Br SCH₃ 7239 SCH₂CH₃ SCH₂CH₃ OCH₂CH₃ Br SCH₃ 7240 N(CH₃)₂ N(CH₃)₂ OCH₂CH₃ Br SCH₃ 7241 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₂CH₃ Br SCH₃ 7242 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₂CH₃ Br SCH₃ 7243 O—(CH₂CH₂)—O OCH₂CH₃ Br SCH₃ 7244 O—(CH₂CH₂CH₂)—O OCH₂CH₃ Br SCH₃ 7245 S—(CH₂CH₂)—S OCH₂CH₃ Br SCH₃ 7246 S—(CH₂CH₂CH₂)—S OCH₂CH₃ Br SCH₃ 7247 —(CH₂)₄— OCH₂CH₃ Br SCH₃ 7248 —(CH₂)₅— OCH₂CH₃ Br SCH₃ 7249 H H SCH₃ Br SCH₃ 7250 CH₃ CH₃ SCH₃ Br SCH₃ 7251 CH₂CH₃ CH₂CH₃ SCH₃ Br SCH₃ 7252 CH₂CH₂CH₃ CH₂CH₂CH₃ SCH₃ Br SCH₃ 7253 OCH₃ OCH₃ SCH₃ Br SCH₃ 7254 OCH₂CH₃ OCH₂CH₃ SCH₃ Br SCH₃ 7255 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SCH₃ Br SCH₃ 7256 SCH₃ SCH₃ SCH₃ Br SCH₃ 7257 SCH₂CH₃ SCH₂CH₃ SCH₃ Br SCH₃ 7258 N(CH₃)₂ N(CH₃)₂ SCH₃ Br SCH₃ 7259 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SCH₃ Br SCH₃ 7260 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SCH₃ Br SCH₃ 7261 O—(CH₂CH₂)—O SCH₃ Br SCH₃ 7262 O—(CH₂CH₂CH₂)—O SCH₃ Br SCH₃ 7263 S—(CH₂CH₂)—S SCH₃ Br SCH₃ 7264 S—(CH₂CH₂CH₂)—S SCH₃ Br SCH₃ 7265 —(CH₂)₄— SCH₃ Br SCH₃ 7266 —(CH₂)₅— SCH₃ Br SCH₃ 7267 H H SO₂CH₃ Br SCH₃ 7268 CH₃ CH₃ SO₂CH₃ Br SCH₃ 7269 CH₂CH₃ CH₂CH₃ SO₂CH₃ Br SCH₃ 7270 CH₂CH₂CH₃ CH₂CH₂CH₃ SO₂CH₃ Br SCH₃ 7271 OCH₃ OCH₃ SO₂CH₃ Br SCH₃ 7272 OCH₂CH₃ OCH₂CH₃ SO₂CH₃ Br SCH₃ 7273 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SO₂CH₃ Br SCH₃ 7274 SCH₃ SCH₃ SO₂CH₃ Br SCH₃ 7275 SCH₂CH₃ SCH₂CH₃ SO₂CH₃ Br SCH₃ 7276 N(CH₃)₂ N(CH₃)₂ SO₂CH₃ Br SCH₃ 7277 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SO₂CH₃ Br SCH₃ 7278 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SO₂CH₃ Br SCH₃ 7279 O—(CH₂CH₂)—O SO₂CH₃ Br SCH₃ 7280 O—(CH₂CH₂CH₂)—O SO₂CH₃ Br SCH₃ 7281 S—(CH₂CH₂)—S SO₂CH₃ Br SCH₃ 7282 S—(CH₂CH₂CH₂)—S SO₂CH₃ Br SCH₃ 7283 —(CH₂)₄— SO₂CH₃ Br SCH₃ 7284 —(CH₂)₅— SO₂CH₃ Br SCH₃ 7285 H H PO(OCH₃)₂ Br SCH₃ 7286 CH₃ CH₃ PO(OCH₃)₂ Br SCH₃ 7287 CH₂CH₃ CH₂CH₃ PO(OCH₃)₂ Br SCH₃ 7288 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₃)₂ Br SCH₃ 7289 OCH₃ OCH₃ PO(OCH₃)₂ Br SCH₃ 7290 OCH₂CH₃ OCH₂CH₃ PO(OCH₃)₂ Br SCH₃ 7291 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₃)₂ Br SCH₃ 7292 SCH₃ SCH₃ PO(OCH₃)₂ Br SCH₃ 7293 SCH₂CH₃ SCH₂CH₃ PO(OCH₃)₂ Br SCH₃ 7294 N(CH₃)₂ N(CH₃)₂ PO(OCH₃)₂ Br SCH₃ 7295 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₃)₂ Br SCH₃ 7296 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₃)₂ Br SCH₃ 7297 O—(CH₂CH₂)—O PO(OCH₃)₂ Br SCH₃ 7298 O—(CH₂CH₂CH₂)—O PO(OCH₃)₂ Br SCH₃ 7299 S—(CH₂CH₂)—S PO(OCH₃)₂ Br SCH₃ 7300 S—(CH₂CH₂CH₂)—S PO(OCH₃)₂ Br SCH₃ 7301 —(CH₂)₄— PO(OCH₃)₂ Br SCH₃ 7302 —(CH₂)₅— PO(OCH₃)₂ Br SCH₃ 7303 H H PO(OCH₂CH₃)₂ Br SCH₃ 7304 CH₃ CH₃ PO(OCH₂CH₃)₂ Br SCH₃ 7305 CH₂CH₃ CH₂CH₃ PO(OCH₂CH₃)₂ Br SCH₃ 7306 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₂CH₃)₂ Br SCH₃ 7307 OCH₃ OCH₃ PO(OCH₂CH₃)₂ Br SCH₃ 7308 OCH₂CH₃ OCH₂CH₃ PO(OCH₂CH₃)₂ Br SCH₃ 7309 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₂CH₃)₂ Br SCH₃ 7310 SCH₃ SCH₃ PO(OCH₂CH₃)₂ Br SCH₃ 7311 SCH₂CH₃ SCH₂CH₃ PO(OCH₂CH₃)₂ Br SCH₃ 7312 N(CH₃)₂ N(CH₃)₂ PO(OCH₂CH₃)₂ Br SCH₃ 7313 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₂CH₃)₂ Br SCH₃ 7314 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₂CH₃)₂ Br SCH₃ 7315 O—(CH₂CH₂)—O PO(OCH₂CH₃)₂ Br SCH₃ 7316 O—(CH₂CH₂CH₂)—O PO(OCH₂CH₃)₂ Br SCH₃ 7317 S—(CH₂CH₂)—S PO(OCH₂CH₃)₂ Br SCH₃ 7318 S—(CH₂CH₂CH₂)—S PO(OCH₂CH₃)₂ Br SCH₃ 7319 —(CH₂)₄— PO(OCH₂CH₃)₂ Br SCH₃ 7320 —(CH₂)₅— PO(OCH₂CH₃)₂ Br SCH₃ 7321 H H PO(CH₃)₂ Br SCH₃ 7322 CH₃ CH₃ PO(CH₃)₂ Br SCH₃ 7323 CH₂CH₃ CH₂CH₃ PO(CH₃)₂ Br SCH₃ 7324 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₃)₂ Br SCH₃ 7325 OCH₃ OCH₃ PO(CH₃)₂ Br SCH₃ 7326 OCH₂CH₃ OCH₂CH₃ PO(CH₃)₂ Br SCH₃ 7327 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₃)₂ Br SCH₃ 7328 SCH₃ SCH₃ PO(CH₃)₂ Br SCH₃ 7329 SCH₂CH₃ SCH₂CH₃ PO(CH₃)₂ Br SCH₃ 7330 N(CH₃)₂ N(CH₃)₂ PO(CH₃)₂ Br SCH₃ 7331 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₃)₂ Br SCH₃ 7332 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₃)₂ Br SCH₃ 7333 O—(CH₂CH₂)—O PO(CH₃)₂ Br SCH₃ 7334 O—(CH₂CH₂CH₂)—O PO(CH₃)₂ Br SCH₃ 7335 S—(CH₂CH₂)—S PO(CH₃)₂ Br SCH₃ 7336 S—(CH₂CH₂CH₂)—S PO(CH₃)₂ Br SCH₃ 7337 —(CH₂)₄— PO(CH₃)₂ Br SCH₃ 7338 —(CH₂)₅— PO(CH₃)₂ Br SCH₃ 7339 H H PC(CH₂CH₃)₂ Br SCH₃ 7340 CH₃ CH₃ PC(CH₂CH₃)₂ Br SCH₃ 7341 CH₂CH₃ CH₂CH₃ PC(CH₂CH₃)₂ Br SCH₃ 7342 CH₂CH₂CH₃ CH₂CH₂CH₃ PC(CH₂CH₃)₂ Br SCH₃ 7343 OCH₃ OCH₃ PC(CH₂CH₃)₂ Br SCH₃ 7344 OCH₂CH₃ OCH₂CH₃ PC(CH₂CH₃)₂ Br SCH₃ 7345 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PC(CH₂CH₃)₂ Br SCH₃ 7346 SCH₃ SCH₃ PC(CH₂CH₃)₂ Br SCH₃ 7347 SCH₂CH₃ SCH₂CH₃ PC(CH₂CH₃)₂ Br SCH₃ 7348 N(CH₃)₂ N(CH₃)₂ PC(CH₂CH₃)₂ Br SCH₃ 7349 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PC(CH₂CH₃)₂ Br SCH₃ 7350 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PC(CH₂CH₃)₂ Br SCH₃ 7351 O—(CH₂CH₂)—O PC(CH₂CH₃)₂ Br SCH₃ 7352 O—(CH₂CH₂CH₂)—O PC(CH₂CH₃)₂ Br SCH₃ 7353 S—(CH₂CH₂)—S PC(CH₂CH₃)₂ Br SCH₃ 7354 S—(CH₂CH₂CH₂)—S PC(CH₂CH₃)₂ Br SCH₃ 7355 —(CH₂)₄— PC(CH₂CH₃)₂ Br SCH₃ 7356 —(CH₂)₅— PC(CH₂CH₃)₂ Br SCH₃ 7357 H H H Br SC₆H₅ 7358 CH₃ CH₃ H Br SC₆H₅ 7359 CH₂CH₃ CH₂CH₃ H Br SC₆H₅ 7360 CH₂CH₂CH₃ CH₂CH₂CH₃ H Br SC₆H₅ 7361 OCH₃ OCH₃ H Br SC₆H₅ 7362 OCH₂CH₃ OCH₂CH₃ H Br SC₆H₅ 7363 OCH₂CH₂CH₃ OCH₂CH₂CH₃ H Br SC₆H₅ 7364 SCH₃ SCH₃ H Br SC₆H₅ 7365 SCH₂CH₃ SCH₂CH₃ H Br SC₆H₅ 7366 N(CH₃)₂ N(CH₃)₂ H Br SC₆H₅ 7367 N(CH₂CH₃)₂ N(CH₂CH₃)₂ H Br SC₆H₅ 7368 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) H Br SC₆H₅ 7369 O—(CH₂CH₂)—O H Br SC₆H₅ 7370 O—(CH₂CH₂CH₂)—O H Br SC₆H₅ 7371 S—(CH₂CH₂)—S H Br SC₆H₅ 7372 S—(CH₂CH₂CH₂)—S H Br SC₆H₅ 7373 —(CH₂)₄— H Br SC₆H₅ 7374 —(CH₂)₅— H Br SC₆H₅ 7375 H H NO₂ Br SC₆H₅ 7376 CH₃ CH₃ NO₂ Br SC₆H₅ 7377 CH₂CH₃ CH₂CH₃ NO₂ Br SC₆H₅ 7378 CH₂CH₂CH₃ CH₂CH₂CH₃ NO₂ Br SC₆H₅ 7379 OCH₃ OCH₃ NO₂ Br SC₆H₅ 7380 OCH₂CH₃ OCH₂CH₃ NO₂ Br SC₆H₅ 7381 OCH₂CH₂CH₃ OCH₂CH₂CH₃ NO₂ Br SC₆H₅ 7382 SCH₃ SCH₃ NO₂ Br SC₆H₅ 7383 SCH₂CH₃ SCH₂CH₃ NO₂ Br SC₆H₅ 7384 N(CH₃)₂ N(CH₃)₂ NO₂ Br SC₆H₅ 7385 N(CH₂CH₃)₂ N(CH₂CH₃)₂ NO₂ Br SC₆H₅ 7386 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) NO₂ Br SC₆H₅ 7387 O—(CH₂CH₂)—O NO₂ Br SC₆H₅ 7388 O—(CH₂CH₂CH₂)—O NO₂ Br SC₆H₅ 7389 S—(CH₂CH₂)—S NO₂ Br SC₆H₅ 7390 S—(CH₂CH₂CH₂)—S NO₂ Br SC₆H₅ 7391 —(CH₂)₄— NO₂ Br SC₆H₅ 7392 —(CH₂)₅— NO₂ Br SC₆H₅ 7393 H H CN Br SC₆H₅ 7394 CH₃ CH₃ CN Br SC₆H₅ 7395 CH₂CH₃ CH₂CH₃ CN Br SC₆H₅ 7396 CH₂CH₂CH₃ CH₂CH₂CH₃ CN Br SC₆H₅ 7397 OCH₃ OCH₃ CN Br SC₆H₅ 7398 OCH₂CH₃ OCH₂CH₃ CN Br SC₆H₅ 7399 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CN Br SC₆H₅ 7400 SCH₃ SCH₃ CN Br SC₆H₅ 7401 SCH₂CH₃ SCH₂CH₃ CN Br SC₆H₅ 7402 N(CH₃)₂ N(CH₃)₂ CN Br SC₆H₅ 7403 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CN Br SC₆H₅ 7404 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CN Br SC₆H₅ 7405 O—(CH₂CH₂)—O CN Br SC₆H₅ 7406 O—(CH₂CH₂CH₂)—O CN Br SC₆H₅ 7407 S—(CH₂CH₂)—S CN Br SC₆H₅ 7408 S—(CH₂CH₂CH₂)—S CN Br SC₆H₅ 7409 —(CH₂)₄— CN Br SC₆H₅ 7410 —(CH₂)₅— CN Br SC₆H₅ 7411 H H F Br SC₆H₅ 7412 CH₃ CH₃ F Br SC₆H₅ 7413 CH₂CH₃ CH₂CH₃ F Br SC₆H₅ 7414 CH₂CH₂CH₃ CH₂CH₂CH₃ F Br SC₆H₅ 7415 OCH₃ OCH₃ F Br SC₆H₅ 7416 OCH₂CH₃ OCH₂CH₃ F Br SC₆H₅ 7417 OCH₂CH₂CH₃ OCH₂CH₂CH₃ F Br SC₆H₅ 7418 SCH₃ SCH₃ F Br SC₆H₅ 7419 SCH₂CH₃ SCH₂CH₃ F Br SC₆H₅ 7420 N(CH₃)₂ N(CH₃)₂ F Br SC₆H₅ 7421 N(CH₂CH₃)₂ N(CH₂CH₃)₂ F Br SC₆H₅ 7422 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) F Br SC₆H₅ 7423 O—(CH₂CH₂)—O F Br SC₆H₅ 7424 O—(CH₂CH₂CH₂)—O F Br SC₆H₅ 7425 S—(CH₂CH₂)—S F Br SC₆H₅ 7426 S—(CH₂CH₂CH₂)—S F Br SC₆H₅ 7427 —(CH₂)₄— F Br SC₆H₅ 7428 —(CH₂)₅— F Br SC₆H₅ 7429 H H Cl Br SC₆H₅ 7430 CH₃ CH₃ Cl Br SC₆H₅ 7431 CH₂CH₃ CH₂CH₃ Cl Br SC₆H₅ 7432 CH₂CH₂CH₃ CH₂CH₂CH₃ Cl Br SC₆H₅ 7433 OCH₃ OCH₃ Cl Br SC₆H₅ 7434 OCH₂CH₃ OCH₂CH₃ Cl Br SC₆H₅ 7435 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Cl Br SC₆H₅ 7436 SCH₃ SCH₃ Cl Br SC₆H₅ 7437 SCH₂CH₃ SCH₂CH₃ Cl Br SC₆H₅ 7438 N(CH₃)₂ N(CH₃)₂ Cl Br SC₆H₅ 7439 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Cl Br SC₆H₅ 7440 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Cl Br SC₆H₅ 7441 O—(CH₂CH₂)—O Cl Br SC₆H₅ 7442 O—(CH₂CH₂CH₂)—O Cl Br SC₆H₅ 7443 S—(CH₂CH₂)—S Cl Br SC₆H₅ 7444 S—(CH₂CH₂CH₂)—S Cl Br SC₆H₅ 7445 —(CH₂)₄— Cl Br SC₆H₅ 7446 —(CH₂)₅— Cl Br SC₆H₅ 7447 H H Br Br SC₆H₅ 7448 CH₃ CH₃ Br Br SC₆H₅ 7449 CH₂CH₃ CH₂CH₃ Br Br SC₆H₅ 7450 CH₂CH₂CH₃ CH₂CH₂CH₃ Br Br SC₆H₅ 7451 OCH₃ OCH₃ Br Br SC₆H₅ 7452 OCH₂CH₃ OCH₂CH₃ Br Br SC₆H₅ 7453 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Br Br SC₆H₅ 7454 SCH₃ SCH₃ Br Br SC₆H₅ 7455 SCH₂CH₃ SCH₂CH₃ Br Br SC₆H₅ 7456 N(CH₃)₂ N(CH₃)₂ Br Br SC₆H₅ 7457 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Br Br SC₆H₅ 7458 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Br Br SC₆H₅ 7459 O—(CH₂CH₂)—O Br Br SC₆H₅ 7460 O—(CH₂CH₂CH₂)—O Br Br SC₆H₅ 7461 S—(CH₂CH₂)—S Br Br SC₆H₅ 7462 S—(CH₂CH₂CH₂)—S Br Br SC₆H₅ 7463 —(CH₂)₄— Br Br SC₆H₅ 7464 —(CH₂)₅— Br Br SC₆H₅ 7465 H H CH₃ Br SC₆H₅ 7466 CH₃ CH₃ CH₃ Br SC₆H₅ 7467 CH₂CH₃ CH₂CH₃ CH₃ Br SC₆H₅ 7468 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₃ Br SC₆H₅ 7469 OCH₃ OCH₃ CH₃ Br SC₆H₅ 7470 OCH₂CH₃ OCH₂CH₃ CH₃ Br SC₆H₅ 7471 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₃ Br SC₆H₅ 7472 SCH₃ SCH₃ CH₃ Br SC₆H₅ 7473 SCH₂CH₃ SCH₂CH₃ CH₃ Br SC₆H₅ 7474 N(CH₃)₂ N(CH₃)₂ CH₃ Br SC₆H₅ 7475 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₃ Br SC₆H₅ 7476 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₃ Br SC₆H₅ 7477 O—(CH₂CH₂)—O CH₃ Br SC₆H₅ 7478 O—(CH₂CH₂CH₂)—O CH₃ Br SC₆H₅ 7479 S—(CH₂CH₂)—S CH₃ Br SC₆H₅ 7480 S—(CH₂CH₂CH₂)—S CH₃ Br SC₆H₅ 7481 —(CH₂)₄— CH₃ Br SC₆H₅ 7482 —(CH₂)₅— CH₃ Br SC₆H₅ 7483 H H CH₂CH₃ Br SC₆H₅ 7484 CH₃ CH₃ CH₂CH₃ Br SC₆H₅ 7485 CH₂CH₃ CH₂CH₃ CH₂CH₃ Br SC₆H₅ 7486 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₂CH₃ Br SC₆H₅ 7487 OCH₃ OCH₃ CH₂CH₃ Br SC₆H₅ 7488 OCH₂CH₃ OCH₂CH₃ CH₂CH₃ Br SC₆H₅ 7489 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₂CH₃ Br SC₆H₅ 7490 SCH₃ SCH₃ CH₂CH₃ Br SC₆H₅ 7491 SCH₂CH₃ SCH₂CH₃ CH₂CH₃ Br SC₆H₅ 7492 N(CH₃)₂ N(CH₃)₂ CH₂CH₃ Br SC₆H₅ 7493 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₂CH₃ Br SC₆H₅ 7494 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₂CH₃ Br SC₆H₅ 7495 O—(CH₂CH₂)—O CH₂CH₃ Br SC₆H₅ 7496 O—(CH₂CH₂CH₂)—O CH₂CH₃ Br SC₆H₅ 7497 S—(CH₂CH₂)—S CH₂CH₃ Br SC₆H₅ 7498 S—(CH₂CH₂CH₂)—S CH₂CH₃ Br SC₆H₅ 7499 —(CH₂)₄— CH₂CH₃ Br SC₆H₅ 7500 —(CH₂)₅— CH₂CH₃ Br SC₆H₅ 7501 H H CF₃ Br SC₆H₅ 7502 CH₃ CH₃ CF₃ Br SC₆H₅ 7503 CH₂CH₃ CH₂CH₃ CF₃ Br SC₆H₅ 7504 CH₂CH₂CH₃ CH₂CH₂CH₃ CF₃ Br SC₆H₅ 7505 OCH₃ OCH₃ CF₃ Br SC₆H₅ 7506 OCH₂CH₃ OCH₂CH₃ CF₃ Br SC₆H₅ 7507 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CF₃ Br SC₆H₅ 7508 SCH₃ SCH₃ CF₃ Br SC₆H₅ 7509 SCH₂CH₃ SCH₂CH₃ CF₃ Br SC₆H₅ 7510 N(CH₃)₂ N(CH₃)₂ CF₃ Br SC₆H₅ 7511 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CF₃ Br SC₆H₅ 7512 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CF₃ Br SC₆H₅ 7513 O—(CH₂CH₂)—O CF₃ Br SC₆H₅ 7514 O—(CH₂CH₂CH₂)—O CF₃ Br SC₆H₅ 7515 S—(CH₂CH₂)—S CF₃ Br SC₆H₅ 7516 S—(CH₂CH₂CH₂)—S CF₃ Br SC₆H₅ 7517 —(CH₂)₄— CF₃ Br SC₆H₅ 7518 —(CH₂)₅— CF₃ Br SC₆H₅ 7519 H H OCH₃ Br SC₆H₅ 7520 CH₃ CH₃ OCH₃ Br SC₆H₅ 7521 CH₂CH₃ CH₂CH₃ OCH₃ Br SC₆H₅ 7522 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₃ Br SC₆H₅ 7523 OCH₃ OCH₃ OCH₃ Br SC₆H₅ 7524 OCH₂CH₃ OCH₂CH₃ OCH₃ Br SC₆H₅ 7525 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₃ Br SC₆H₅ 7526 SCH₃ SCH₃ OCH₃ Br SC₆H₅ 7527 SCH₂CH₃ SCH₂CH₃ OCH₃ Br SC₆H₅ 7528 N(CH₃)₂ N(CH₃)₂ OCH₃ Br SC₆H₅ 7529 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₃ Br SC₆H₅ 7530 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₃ Br SC₆H₅ 7531 O—(CH₂CH₂)—O OCH₃ Br SC₆H₅ 7532 O—(CH₂CH₂CH₂)—O OCH₃ Br SC₆H₅ 7533 S—(CH₂CH₂)—S OCH₃ Br SC₆H₅ 7534 S—(CH₂CH₂CH₂)—S OCH₃ Br SC₆H₅ 7535 —(CH₂)₄— OCH₃ Br SC₆H₅ 7536 —(CH₂)₅— OCH₃ Br SC₆H₅ 7537 H H OCH₂CH₃ Br SC₆H₅ 7538 CH₃ CH₃ OCH₂CH₃ Br SC₆H₅ 7539 CH₂CH₃ CH₂CH₃ OCH₂CH₃ Br SC₆H₅ 7540 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₂CH₃ Br SC₆H₅ 7541 OCH₃ OCH₃ OCH₂CH₃ Br SC₆H₅ 7542 OCH₂CH₃ OCH₂CH₃ OCH₂CH₃ Br SC₆H₅ 7543 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₂CH₃ Br SC₆H₅ 7544 SCH₃ SCH₃ OCH₂CH₃ Br SC₆H₅ 7545 SCH₂CH₃ SCH₂CH₃ OCH₂CH₃ Br SC₆H₅ 7546 N(CH₃)₂ N(CH₃)₂ OCH₂CH₃ Br SC₆H₅ 7547 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₂CH₃ Br SC₆H₅ 7548 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₂CH₃ Br SC₆H₅ 7549 O—(CH₂CH₂)—O OCH₂CH₃ Br SC₆H₅ 7550 O—(CH₂CH₂CH₂)—O OCH₂CH₃ Br SC₆H₅ 7551 S—(CH₂CH₂)—S OCH₂CH₃ Br SC₆H₅ 7552 S—(CH₂CH₂CH₂)—S OCH₂CH₃ Br SC₆H₅ 7553 —(CH₂)₄— OCH₂CH₃ Br SC₆H₅ 7554 —(CH₂)₅— OCH₂CH₃ Br SC₆H₅ 7555 H H SCH₃ Br SC₆H₅ 7556 CH₃ CH₃ SCH₃ Br SC₆H₅ 7557 CH₂CH₃ CH₂CH₃ SCH₃ Br SC₆H₅ 7558 CH₂CH₂CH₃ CH₂CH₂CH₃ SCH₃ Br SC₆H₅ 7559 OCH₃ OCH₃ SCH₃ Br SC₆H₅ 7560 OCH₂CH₃ OCH₂CH₃ SCH₃ Br SC₆H₅ 7561 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SCH₃ Br SC₆H₅ 7562 SCH₃ SCH₃ SCH₃ Br SC₆H₅ 7563 SCH₂CH₃ SCH₂CH₃ SCH₃ Br SC₆H₅ 7564 N(CH₃)₂ N(CH₃)₂ SCH₃ Br SC₆H₅ 7565 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SCH₃ Br SC₆H₅ 7566 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SCH₃ Br SC₆H₅ 7567 O—(CH₂CH₂)—O SCH₃ Br SC₆H₅ 7568 O—(CH₂CH₂CH₂)—O SCH₃ Br SC₆H₅ 7569 S—(CH₂CH₂)—S SCH₃ Br SC₆H₅ 7570 S—(CH₂CH₂CH₂)—S SCH₃ Br SC₆H₅ 7571 —(CH₂)₄— SCH₃ Br SC₆H₅ 7572 —(CH₂)₅— SCH₃ Br SC₆H₅ 7573 H H SO₂CH₃ Br SC₆H₅ 7574 CH₃ CH₃ SO₂CH₃ Br SC₆H₅ 7575 CH₂CH₃ CH₂CH₃ SO₂CH₃ Br SC₆H₅ 7576 CH₂CH₂CH₃ CH₂CH₂CH₃ SO₂CH₃ Br SC₆H₅ 7577 OCH₃ OCH₃ SO₂CH₃ Br SC₆H₅ 7578 OCH₂CH₃ OCH₂CH₃ SO₂CH₃ Br SC₆H₅ 7579 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SO₂CH₃ Br SC₆H₅ 7580 SCH₃ SCH₃ SO₂CH₃ Br SC₆H₅ 7581 SCH₂CH₃ SCH₂CH₃ SO₂CH₃ Br SC₆H₅ 7582 N(CH₃)₂ N(CH₃)₂ SO₂CH₃ Br SC₆H₅ 7583 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SO₂CH₃ Br SC₆H₅ 7584 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SO₂CH₃ Br SC₆H₅ 7585 O—(CH₂CH₂)—O SO₂CH₃ Br SC₆H₅ 7586 O—(CH₂CH₂CH₂)—O SO₂CH₃ Br SC₆H₅ 7587 S—(CH₂CH₂)—S SO₂CH₃ Br SC₆H₅ 7588 S—(CH₂CH₂CH₂)—S SO₂CH₃ Br SC₆H₅ 7589 —(CH₂)₄— SO₂CH₃ Br SC₆H₅ 7590 —(CH₂)₅— SO₂CH₃ Br SC₆H₅ 7591 H H PO(OCH₃)₂ Br SC₆H₅ 7592 CH₃ CH₃ PO(OCH₃)₂ Br SC₆H₅ 7593 CH₂CH₃ CH₂CH₃ PO(OCH₃)₂ Br SC₆H₅ 7594 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₃)₂ Br SC₆H₅ 7595 OCH₃ OCH₃ PO(OCH₃)₂ Br SC₆H₅ 7596 OCH₂CH₃ OCH₂CH₃ PO(OCH₃)₂ Br SC₆H₅ 7597 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₃)₂ Br SC₆H₅ 7598 SCH₃ SCH₃ PO(OCH₃)₂ Br SC₆H₅ 7599 SCH₂CH₃ SCH₂CH₃ PO(OCH₃)₂ Br SC₆H₅ 7600 N(CH₃)₂ N(CH₃)₂ PO(OCH₃)₂ Br SC₆H₅ 7601 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₃)₂ Br SC₆H₅ 7602 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₃)₂ Br SC₆H₅ 7603 O—(CH₂CH₂)—O PO(OCH₃)₂ Br SC₆H₅ 7604 O—(CH₂CH₂CH₂)—O PO(OCH₃)₂ Br SC₆H₅ 7605 S—(CH₂CH₂)—S PO(OCH₃)₂ Br SC₆H₅ 7606 S—(CH₂CH₂CH₂)—S PO(OCH₃)₂ Br SC₆H₅ 7607 —(CH₂)₄— PO(OCH₃)₂ Br SC₆H₅ 7608 —(CH₂)₅— PO(OCH₃)₂ Br SC₆H₅ 7609 H H PO(OCH₂CH₃)₂ Br SC₆H₅ 7610 CH₃ CH₃ PO(OCH₂CH₃)₂ Br SC₆H₅ 7611 CH₂CH₃ CH₂CH₃ PO(OCH₂CH₃)₂ Br SC₆H₅ 7612 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₂CH₃)₂ Br SC₆H₅ 7613 OCH₃ OCH₃ PO(OCH₂CH₃)₂ Br SC₆H₅ 7614 OCH₂CH₃ OCH₂CH₃ PO(OCH₂CH₃)₂ Br SC₆H₅ 7615 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₂CH₃)₂ Br SC₆H₅ 7616 SCH₃ SCH₃ PO(OCH₂CH₃)₂ Br SC₆H₅ 7617 SCH₂CH₃ SCH₂CH₃ PO(OCH₂CH₃)₂ Br SC₆H₅ 7618 N(CH₃)₂ N(CH₃)₂ PO(OCH₂CH₃)₂ Br SC₆H₅ 7619 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₂CH₃)₂ Br SC₆H₅ 7620 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₂CH₃)₂ Br SC₆H₅ 7621 O—(CH₂CH₂)—O PO(OCH₂CH₃)₂ Br SC₆H₅ 7622 O—(CH₂CH₂CH₂)—O PO(OCH₂CH₃)₂ Br SC₆H₅ 7623 S—(CH₂CH₂)—S PO(OCH₂CH₃)₂ Br SC₆H₅ 7624 S—(CH₂CH₂CH₂)—S PO(OCH₂CH₃)₂ Br SC₆H₅ 7625 —(CH₂)₄— PO(OCH₂CH₃)₂ Br SC₆H₅ 7626 —(CH₂)₅— PO(OCH₂CH₃)₂ Br SC₆H₅ 7627 H H PO(CH₃)₂ Br SC₆H₅ 7628 CH₃ CH₃ PO(CH₃)₂ Br SC₆H₅ 7629 CH₂CH₃ CH₂CH₃ PO(CH₃)₂ Br SC₆H₅ 7630 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₃)₂ Br SC₆H₅ 7631 OCH₃ OCH₃ PO(CH₃)₂ Br SC₆H₅ 7632 OCH₂CH₃ OCH₂CH₃ PO(CH₃)₂ Br SC₆H₅ 7633 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₃)₂ Br SC₆H₅ 7634 SCH₃ SCH₃ PO(CH₃)₂ Br SC₆H₅ 7635 SCH₂CH₃ SCH₂CH₃ PO(CH₃)₂ Br SC₆H₅ 7636 N(CH₃)₂ N(CH₃)₂ PO(CH₃)₂ Br SC₆H₅ 7637 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₃)₂ Br SC₆H₅ 7638 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₃)₂ Br SC₆H₅ 7639 O—(CH₂CH₂)—O PO(CH₃)₂ Br SC₆H₅ 7640 O—(CH₂CH₂CH₂)—O PO(CH₃)₂ Br SC₆H₅ 7641 S—(CH₂CH₂)—S PO(CH₃)₂ Br SC₆H₅ 7642 S—(CH₂CH₂CH₂)—S PO(CH₃)₂ Br SC₆H₅ 7643 —(CH₂)₄— PO(CH₃)₂ Br SC₆H₅ 7644 —(CH₂)₅— PO(CH₃)₂ Br SC₆H₅ 7645 H H PC(CH₂CH₃)₂ Br SC₆H₅ 7646 CH₃ CH₃ PC(CH₂CH₃)₂ Br SC₆H₅ 7647 CH₂CH₃ CH₂CH₃ PC(CH₂CH₃)₂ Br SC₆H₅ 7648 CH₂CH₂CH₃ CH₂CH₂CH₃ PC(CH₂CH₃)₂ Br SC₆H₅ 7649 OCH₃ OCH₃ PC(CH₂CH₃)₂ Br SC₆H₅ 7650 OCH₂CH₃ OCH₂CH₃ PC(CH₂CH₃)₂ Br SC₆H₅ 7651 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PC(CH₂CH₃)₂ Br SC₆H₅ 7652 SCH₃ SCH₃ PC(CH₂CH₃)₂ Br SC₆H₅ 7653 SCH₂CH₃ SCH₂CH₃ PC(CH₂CH₃)₂ Br SC₆H₅ 7654 N(CH₃)₂ N(CH₃)₂ PC(CH₂CH₃)₂ Br SC₆H₅ 7655 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PC(CH₂CH₃)₂ Br SC₆H₅ 7656 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PC(CH₂CH₃)₂ Br SC₆H₅ 7657 O—(CH₂CH₂)—O PC(CH₂CH₃)₂ Br SC₆H₅ 7658 O—(CH₂CH₂CH₂)—O PC(CH₂CH₃)₂ Br SC₆H₅ 7659 S—(CH₂CH₂)—S PC(CH₂CH₃)₂ Br SC₆H₅ 7660 S—(CH₂CH₂CH₂)—S PC(CH₂CH₃)₂ Br SC₆H₅ 7661 —(CH₂)₄— PC(CH₂CH₃)₂ Br SC₆H₅ 7662 —(CH₂)₅— PC(CH₂CH₃)₂ Br SC₆H₅ 7663 H H H Br Het1 7664 CH₃ CH₃ H Br Het1 7665 CH₂CH₃ CH₂CH₃ H Br Het1 7666 CH₂CH₂CH₃ CH₂CH₂CH₃ H Br Het1 7667 OCH₃ OCH₃ H Br Het1 7668 OCH₂CH₃ OCH₂CH₃ H Br Het1 7669 OCH₂CH₂CH₃ OCH₂CH₂CH₃ H Br Het1 7670 SCH₃ SCH₃ H Br Het1 7671 SCH₂CH₃ SCH₂CH₃ H Br Het1 7672 N(CH₃)₂ N(CH₃)₂ H Br Het1 7673 N(CH₂CH₃)₂ N(CH₂CH₃)₂ H Br Het1 7674 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) H Br Het1 7675 O—(CH₂CH₂)—O H Br Het1 7676 O—(CH₂CH₂CH₂)—O H Br Het1 7677 S—(CH₂CH₂)—S H Br Het1 7678 S—(CH₂CH₂CH₂)—S H Br Het1 7679 —(CH₂)₄— H Br Het1 7680 —(CH₂)₅— H Br Het1 7681 H H NO₂ Br Het1 7682 CH₃ CH₃ NO₂ Br Het1 7683 CH₂CH₃ CH₂CH₃ NO₂ Br Het1 7684 CH₂CH₂CH₃ CH₂CH₂CH₃ NO₂ Br Het1 7685 OCH₃ OCH₃ NO₂ Br Het1 7686 OCH₂CH₃ OCH₂CH₃ NO₂ Br Het1 7687 OCH₂CH₂CH₃ OCH₂CH₂CH₃ NO₂ Br Het1 7688 SCH₃ SCH₃ NO₂ Br Het1 7689 SCH₂CH₃ SCH₂CH₃ NO₂ Br Het1 7690 N(CH₃)₂ N(CH₃)₂ NO₂ Br Het1 7691 N(CH₂CH₃)₂ N(CH₂CH₃)₂ NO₂ Br Het1 7692 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) NO₂ Br Het1 7693 O—(CH₂CH₂)—O NO₂ Br Het1 7694 O—(CH₂CH₂CH₂)—O NO₂ Br Het1 7695 S—(CH₂CH₂)—S NO₂ Br Het1 7696 S—(CH₂CH₂CH₂)—S NO₂ Br Het1 7697 —(CH₂)₄— NO₂ Br Het1 7698 —(CH₂)₅— NO₂ Br Het1 7699 H H CN Br Het1 7700 CH₃ CH₃ CN Br Het1 7701 CH₂CH₃ CH₂CH₃ CN Br Het1 7702 CH₂CH₂CH₃ CH₂CH₂CH₃ CN Br Het1 7703 OCH₃ OCH₃ CN Br Het1 7704 OCH₂CH₃ OCH₂CH₃ CN Br Het1 7705 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CN Br Het1 7706 SCH₃ SCH₃ CN Br Het1 7707 SCH₂CH₃ SCH₂CH₃ CN Br Het1 7708 N(CH₃)₂ N(CH₃)₂ CN Br Het1 7709 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CN Br Het1 7710 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CN Br Het1 7711 O—(CH₂CH₂)—O CN Br Het1 7712 O—(CH₂CH₂CH₂)—O CN Br Het1 7713 S—(CH₂CH₂)—S CN Br Het1 7714 S—(CH₂CH₂CH₂)—S CN Br Het1 7715 —(CH₂)₄— CN Br Het1 7716 —(CH₂)₅— CN Br Het1 7717 H H F Br Het1 7718 CH₃ CH₃ F Br Het1 7719 CH₂CH₃ CH₂CH₃ F Br Het1 7720 CH₂CH₂CH₃ CH₂CH₂CH₃ F Br Het1 7721 OCH₃ OCH₃ F Br Het1 7722 OCH₂CH₃ OCH₂CH₃ F Br Het1 7723 OCH₂CH₂CH₃ OCH₂CH₂CH₃ F Br Het1 7724 SCH₃ SCH₃ F Br Het1 7725 SCH₂CH₃ SCH₂CH₃ F Br Het1 7726 N(CH₃)₂ N(CH₃)₂ F Br Het1 7727 N(CH₂CH₃)₂ N(CH₂CH₃)₂ F Br Het1 7728 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) F Br Het1 7729 O—(CH₂CH₂)—O F Br Het1 7730 O—(CH₂CH₂CH₂)—O F Br Het1 7731 S—(CH₂CH₂)—S F Br Het1 7732 S—(CH₂CH₂CH₂)—S F Br Het1 7733 —(CH₂)₄— F Br Het1 7734 —(CH₂)₅— F Br Het1 7735 H H Cl Br Het1 7736 CH₃ CH₃ Cl Br Het1 7737 CH₂CH₃ CH₂CH₃ Cl Br Het1 7738 CH₂CH₂CH₃ CH₂CH₂CH₃ Cl Br Het1 7739 OCH₃ OCH₃ Cl Br Het1 7740 OCH₂CH₃ OCH₂CH₃ Cl Br Het1 7741 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Cl Br Het1 7742 SCH₃ SCH₃ Cl Br Het1 7743 SCH₂CH₃ SCH₂CH₃ Cl Br Het1 7744 N(CH₃)₂ N(CH₃)₂ Cl Br Het1 7745 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Cl Br Het1 7746 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Cl Br Het1 7747 O—(CH₂CH₂)—O Cl Br Het1 7748 O—(CH₂CH₂CH₂)—O Cl Br Het1 7749 S—(CH₂CH₂)—S Cl Br Het1 7750 S—(CH₂CH₂CH₂)—S Cl Br Het1 7751 —(CH₂)₄— Cl Br Het1 7752 —(CH₂)₅— Cl Br Het1 7753 H H Br Br Het1 7754 CH₃ CH₃ Br Br Het1 7755 CH₂CH₃ CH₂CH₃ Br Br Het1 7756 CH₂CH₂CH₃ CH₂CH₂CH₃ Br Br Het1 7757 OCH₃ OCH₃ Br Br Het1 7758 OCH₂CH₃ OCH₂CH₃ Br Br Het1 7759 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Br Br Het1 7760 SCH₃ SCH₃ Br Br Het1 7761 SCH₂CH₃ SCH₂CH₃ Br Br Het1 7762 N(CH₃)₂ N(CH₃)₂ Br Br Het1 7763 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Br Br Het1 7764 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Br Br Het1 7765 O—(CH₂CH₂)—O Br Br Het1 7766 O—(CH₂CH₂CH₂)—O Br Br Het1 7767 S—(CH₂CH₂)—S Br Br Het1 7768 S—(CH₂CH₂CH₂)—S Br Br Het1 7769 —(CH₂)₄— Br Br Het1 7770 —(CH₂)₅— Br Br Het1 7771 H H CH₃ Br Het1 7772 CH₃ CH₃ CH₃ Br Het1 7773 CH₂CH₃ CH₂CH₃ CH₃ Br Het1 7774 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₃ Br Het1 7775 OCH₃ OCH₃ CH₃ Br Het1 7776 OCH₂CH₃ OCH₂CH₃ CH₃ Br Het1 7777 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₃ Br Het1 7778 SCH₃ SCH₃ CH₃ Br Het1 7779 SCH₂CH₃ SCH₂CH₃ CH₃ Br Het1 7780 N(CH₃)₂ N(CH₃)₂ CH₃ Br Het1 7781 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₃ Br Het1 7782 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₃ Br Het1 7783 O—(CH₂CH₂)—O CH₃ Br Het1 7784 O—(CH₂CH₂CH₂)—O CH₃ Br Het1 7785 S—(CH₂CH₂)—S CH₃ Br Het1 7786 S—(CH₂CH₂CH₂)—S CH₃ Br Het1 7787 —(CH₂)₄— CH₃ Br Het1 7788 —(CH₂)₅— CH₃ Br Het1 7789 H H CH₂CH₃ Br Het1 7790 CH₃ CH₃ CH₂CH₃ Br Het1 7791 CH₂CH₃ CH₂CH₃ CH₂CH₃ Br Het1 7792 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₂CH₃ Br Het1 7793 OCH₃ OCH₃ CH₂CH₃ Br Het1 7794 OCH₂CH₃ OCH₂CH₃ CH₂CH₃ Br Het1 7795 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₂CH₃ Br Het1 7796 SCH₃ SCH₃ CH₂CH₃ Br Het1 7797 SCH₂CH₃ SCH₂CH₃ CH₂CH₃ Br Het1 7798 N(CH₃)₂ N(CH₃)₂ CH₂CH₃ Br Het1 7799 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₂CH₃ Br Het1 7800 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₂CH₃ Br Het1 7801 O—(CH₂CH₂)—O CH₂CH₃ Br Het1 7802 O—(CH₂CH₂CH₂)—O CH₂CH₃ Br Het1 7803 S—(CH₂CH₂)—S CH₂CH₃ Br Het1 7804 S—(CH₂CH₂CH₂)—S CH₂CH₃ Br Het1 7805 —(CH₂)₄— CH₂CH₃ Br Het1 7806 —(CH₂)₅— CH₂CH₃ Br Het1 7807 H H CF₃ Br Het1 7808 CH₃ CH₃ CF₃ Br Het1 7809 CH₂CH₃ CH₂CH₃ CF₃ Br Het1 7810 CH₂CH₂CH₃ CH₂CH₂CH₃ CF₃ Br Het1 7811 OCH₃ OCH₃ CF₃ Br Het1 7812 OCH₂CH₃ OCH₂CH₃ CF₃ Br Het1 7813 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CF₃ Br Het1 7814 SCH₃ SCH₃ CF₃ Br Het1 7815 SCH₂CH₃ SCH₂CH₃ CF₃ Br Het1 7816 N(CH₃)₂ N(CH₃)₂ CF₃ Br Het1 7817 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CF₃ Br Het1 7818 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CF₃ Br Het1 7819 O—(CH₂CH₂)—O CF₃ Br Het1 7820 O—(CH₂CH₂CH₂)—O CF₃ Br Het1 7821 S—(CH₂CH₂)—S CF₃ Br Het1 7822 S—(CH₂CH₂CH₂)—S CF₃ Br Het1 7823 —(CH₂)₄— CF₃ Br Het1 7824 —(CH₂)₅— CF₃ Br Het1 7825 H H OCH₃ Br Het1 7826 CH₃ CH₃ OCH₃ Br Het1 7827 CH₂CH₃ CH₂CH₃ OCH₃ Br Het1 7828 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₃ Br Het1 7829 OCH₃ OCH₃ OCH₃ Br Het1 7830 OCH₂CH₃ OCH₂CH₃ OCH₃ Br Het1 7831 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₃ Br Het1 7832 SCH₃ SCH₃ OCH₃ Br Het1 7833 SCH₂CH₃ SCH₂CH₃ OCH₃ Br Het1 7834 N(CH₃)₂ N(CH₃)₂ OCH₃ Br Het1 7835 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₃ Br Het1 7836 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₃ Br Het1 7837 O—(CH₂CH₂)—O OCH₃ Br Het1 7838 O—(CH₂CH₂CH₂)—O OCH₃ Br Het1 7839 S—(CH₂CH₂)—S OCH₃ Br Het1 7840 S—(CH₂CH₂CH₂)—S OCH₃ Br Het1 7841 —(CH₂)₄— OCH₃ Br Het1 7842 —(CH₂)₅— OCH₃ Br Het1 7843 H H OCH₂CH₃ Br Het1 7844 CH₃ CH₃ OCH₂CH₃ Br Het1 7845 CH₂CH₃ CH₂CH₃ OCH₂CH₃ Br Het1 7846 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₂CH₃ Br Het1 7847 OCH₃ OCH₃ OCH₂CH₃ Br Het1 7848 OCH₂CH₃ OCH₂CH₃ OCH₂CH₃ Br Het1 7849 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₂CH₃ Br Het1 7850 SCH₃ SCH₃ OCH₂CH₃ Br Het1 7851 SCH₂CH₃ SCH₂CH₃ OCH₂CH₃ Br Het1 7852 N(CH₃)₂ N(CH₃)₂ OCH₂CH₃ Br Het1 7853 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₂CH₃ Br Het1 7854 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₂CH₃ Br Het1 7855 O—(CH₂CH₂)—O OCH₂CH₃ Br Het1 7856 O—(CH₂CH₂CH₂)—O OCH₂CH₃ Br Het1 7857 S—(CH₂CH₂)—S OCH₂CH₃ Br Het1 7858 S—(CH₂CH₂CH₂)—S OCH₂CH₃ Br Het1 7859 —(CH₂)₄— OCH₂CH₃ Br Het1 7860 —(CH₂)₅— OCH₂CH₃ Br Het1 7861 H H SCH₃ Br Het1 7862 CH₃ CH₃ SCH₃ Br Het1 7863 CH₂CH₃ CH₂CH₃ SCH₃ Br Het1 7864 CH₂CH₂CH₃ CH₂CH₂CH₃ SCH₃ Br Het1 7865 OCH₃ OCH₃ SCH₃ Br Het1 7866 OCH₂CH₃ OCH₂CH₃ SCH₃ Br Het1 7867 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SCH₃ Br Het1 7868 SCH₃ SCH₃ SCH₃ Br Het1 7869 SCH₂CH₃ SCH₂CH₃ SCH₃ Br Het1 7870 N(CH₃)₂ N(CH₃)₂ SCH₃ Br Het1 7871 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SCH₃ Br Het1 7872 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SCH₃ Br Het1 7873 O—(CH₂CH₂)—O SCH₃ Br Het1 7874 O—(CH₂CH₂CH₂)—O SCH₃ Br Het1 7875 S—(CH₂CH₂)—S SCH₃ Br Het1 7876 S—(CH₂CH₂CH₂)—S SCH₃ Br Het1 7877 —(CH₂)₄— SCH₃ Br Het1 7878 —(CH₂)₅— SCH₃ Br Het1 7879 H H SO₂CH₃ Br Het1 7880 CH₃ CH₃ SO₂CH₃ Br Het1 7881 CH₂CH₃ CH₂CH₃ SO₂CH₃ Br Het1 7882 CH₂CH₂CH₃ CH₂CH₂CH₃ SO₂CH₃ Br Het1 7883 OCH₃ OCH₃ SO₂CH₃ Br Het1 7884 OCH₂CH₃ OCH₂CH₃ SO₂CH₃ Br Het1 7885 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SO₂CH₃ Br Het1 7886 SCH₃ SCH₃ SO₂CH₃ Br Het1 7887 SCH₂CH₃ SCH₂CH₃ SO₂CH₃ Br Het1 7888 N(CH₃)₂ N(CH₃)₂ SO₂CH₃ Br Het1 7889 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SO₂CH₃ Br Het1 7890 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SO₂CH₃ Br Het1 7891 O—(CH₂CH₂)—O SO₂CH₃ Br Het1 7892 O—(CH₂CH₂CH₂)—O SO₂CH₃ Br Het1 7893 S—(CH₂CH₂)—S SO₂CH₃ Br Het1 7894 S—(CH₂CH₂CH₂)—S SO₂CH₃ Br Het1 7895 —(CH₂)₄— SO₂CH₃ Br Het1 7896 —(CH₂)₅— SO₂CH₃ Br Het1 7897 H H PO(OCH₃)₂ Br Het1 7898 CH₃ CH₃ PO(OCH₃)₂ Br Het1 7899 CH₂CH₃ CH₂CH₃ PO(OCH₃)₂ Br Het1 7900 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₃)₂ Br Het1 7901 OCH₃ OCH₃ PO(OCH₃)₂ Br Het1 7902 OCH₂CH₃ OCH₂CH₃ PO(OCH₃)₂ Br Het1 7903 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₃)₂ Br Het1 7904 SCH₃ SCH₃ PO(OCH₃)₂ Br Het1 7905 SCH₂CH₃ SCH₂CH₃ PO(OCH₃)₂ Br Het1 7906 N(CH₃)₂ N(CH₃)₂ PO(OCH₃)₂ Br Het1 7907 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₃)₂ Br Het1 7908 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₃)₂ Br Het1 7909 O—(CH₂CH₂)—O PO(OCH₃)₂ Br Het1 7910 O—(CH₂CH₂CH₂)—O PO(OCH₃)₂ Br Het1 7911 S—(CH₂CH₂)—S PO(OCH₃)₂ Br Het1 7912 S—(CH₂CH₂CH₂)—S PO(OCH₃)₂ Br Het1 7913 —(CH₂)₄— PO(OCH₃)₂ Br Het1 7914 —(CH₂)₅— PO(OCH₃)₂ Br Het1 7915 H H PO(OCH₂CH₃)₂ Br Het1 7916 CH₃ CH₃ PO(OCH₂CH₃)₂ Br Het1 7917 CH₂CH₃ CH₂CH₃ PO(OCH₂CH₃)₂ Br Het1 7918 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₂CH₃)₂ Br Het1 7919 OCH₃ OCH₃ PO(OCH₂CH₃)₂ Br Het1 7920 OCH₂CH₃ OCH₂CH₃ PO(OCH₂CH₃)₂ Br Het1 7921 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₂CH₃)₂ Br Het1 7922 SCH₃ SCH₃ PO(OCH₂CH₃)₂ Br Het1 7923 SCH₂CH₃ SCH₂CH₃ PO(OCH₂CH₃)₂ Br Het1 7924 N(CH₃)₂ N(CH₃)₂ PO(OCH₂CH₃)₂ Br Het1 7925 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₂CH₃)₂ Br Het1 7926 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₂CH₃)₂ Br Het1 7927 O—(CH₂CH₂)—O PO(OCH₂CH₃)₂ Br Het1 7928 O—(CH₂CH₂CH₂)—O PO(OCH₂CH₃)₂ Br Het1 7929 S—(CH₂CH₂)—S PO(OCH₂CH₃)₂ Br Het1 7930 S—(CH₂CH₂CH₂)—S PO(OCH₂CH₃)₂ Br Het1 7931 —(CH₂)₄— PO(OCH₂CH₃)₂ Br Het1 7932 —(CH₂)₅— PO(OCH₂CH₃)₂ Br Het1 7933 H H PO(CH₃)₂ Br Het1 7934 CH₃ CH₃ PO(CH₃)₂ Br Het1 7935 CH₂CH₃ CH₂CH₃ PO(CH₃)₂ Br Het1 7936 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₃)₂ Br Het1 7937 OCH₃ OCH₃ PO(CH₃)₂ Br Het1 7938 OCH₂CH₃ OCH₂CH₃ PO(CH₃)₂ Br Het1 7939 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₃)₂ Br Het1 7940 SCH₃ SCH₃ PO(CH₃)₂ Br Het1 7941 SCH₂CH₃ SCH₂CH₃ PO(CH₃)₂ Br Het1 7942 N(CH₃)₂ N(CH₃)₂ PO(CH₃)₂ Br Het1 7943 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₃)₂ Br Het1 7944 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₃)₂ Br Het1 7945 O—(CH₂CH₂)—O PO(CH₃)₂ Br Het1 7946 O—(CH₂CH₂CH₂)—O PO(CH₃)₂ Br Het1 7947 S—(CH₂CH₂)—S PO(CH₃)₂ Br Het1 7948 S—(CH₂CH₂CH₂)—S PO(CH₃)₂ Br Het1 7949 —(CH₂)₄— PO(CH₃)₂ Br Het1 7950 —(CH₂)₅— PO(CH₃)₂ Br Het1 7951 H H PC(CH₂CH₃)₂ Br Het1 7952 CH₃ CH₃ PC(CH₂CH₃)₂ Br Het1 7953 CH₂CH₃ CH₂CH₃ PC(CH₂CH₃)₂ Br Het1 7954 CH₂CH₂CH₃ CH₂CH₂CH₃ PC(CH₂CH₃)₂ Br Het1 7955 OCH₃ OCH₃ PC(CH₂CH₃)₂ Br Het1 7956 OCH₂CH₃ OCH₂CH₃ PC(CH₂CH₃)₂ Br Het1 7957 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PC(CH₂CH₃)₂ Br Het1 7958 SCH₃ SCH₃ PC(CH₂CH₃)₂ Br Het1 7959 SCH₂CH₃ SCH₂CH₃ PC(CH₂CH₃)₂ Br Het1 7960 N(CH₃)₂ N(CH₃)₂ PC(CH₂CH₃)₂ Br Het1 7961 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PC(CH₂CH₃)₂ Br Het1 7962 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PC(CH₂CH₃)₂ Br Het1 7963 O—(CH₂CH₂)—O PC(CH₂CH₃)₂ Br Het1 7964 O—(CH₂CH₂CH₂)—O PC(CH₂CH₃)₂ Br Het1 7965 S—(CH₂CH₂)—S PC(CH₂CH₃)₂ Br Het1 7966 S—(CH₂CH₂CH₂)—S PC(CH₂CH₃)₂ Br Het1 7967 —(CH₂)₄— PC(CH₂CH₃)₂ Br Het1 7968 —(CH₂)₅— PC(CH₂CH₃)₂ Br Het1 7969 H H H Br Het2 7970 CH₃ CH₃ H Br Het2 7971 CH₂CH₃ CH₂CH₃ H Br Het2 7972 CH₂CH₂CH₃ CH₂CH₂CH₃ H Br Het2 7973 OCH₃ OCH₃ H Br Het2 7974 OCH₂CH₃ OCH₂CH₃ H Br Het2 7975 OCH₂CH₂CH₃ OCH₂CH₂CH₃ H Br Het2 7976 SCH₃ SCH₃ H Br Het2 7977 SCH₂CH₃ SCH₂CH₃ H Br Het2 7978 N(CH₃)₂ N(CH₃)₂ H Br Het2 7979 N(CH₂CH₃)₂ N(CH₂CH₃)₂ H Br Het2 7980 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) H Br Het2 7981 O—(CH₂CH₂)—O H Br Het2 7982 O—(CH₂CH₂CH₂)—O H Br Het2 7983 S—(CH₂CH₂)—S H Br Het2 7984 S—(CH₂CH₂CH₂)—S H Br Het2 7985 —(CH₂)₄— H Br Het2 7986 —(CH₂)₅— H Br Het2 7987 H H NO₂ Br Het2 7988 CH₃ CH₃ NO₂ Br Het2 7989 CH₂CH₃ CH₂CH₃ NO₂ Br Het2 7990 CH₂CH₂CH₃ CH₂CH₂CH₃ NO₂ Br Het2 7991 OCH₃ OCH₃ NO₂ Br Het2 7992 OCH₂CH₃ OCH₂CH₃ NO₂ Br Het2 7993 OCH₂CH₂CH₃ OCH₂CH₂CH₃ NO₂ Br Het2 7994 SCH₃ SCH₃ NO₂ Br Het2 7995 SCH₂CH₃ SCH₂CH₃ NO₂ Br Het2 7996 N(CH₃)₂ N(CH₃)₂ NO₂ Br Het2 7997 N(CH₂CH₃)₂ N(CH₂CH₃)₂ NO₂ Br Het2 7998 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) NO₂ Br Het2 7999 O—(CH₂CH₂)—O NO₂ Br Het2 8000 O—(CH₂CH₂CH₂)—O NO₂ Br Het2 8001 S—(CH₂CH₂)—S NO₂ Br Het2 8002 S—(CH₂CH₂CH₂)—S NO₂ Br Het2 8003 —(CH₂)₄— NO₂ Br Het2 8004 —(CH₂)₅— NO₂ Br Het2 8005 H H CN Br Het2 8006 CH₃ CH₃ CN Br Het2 8007 CH₂CH₃ CH₂CH₃ CN Br Het2 8008 CH₂CH₂CH₃ CH₂CH₂CH₃ CN Br Het2 8009 OCH₃ OCH₃ CN Br Het2 8010 OCH₂CH₃ OCH₂CH₃ CN Br Het2 8011 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CN Br Het2 8012 SCH₃ SCH₃ CN Br Het2 8013 SCH₂CH₃ SCH₂CH₃ CN Br Het2 8014 N(CH₃)₂ N(CH₃)₂ CN Br Het2 8015 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CN Br Het2 8016 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CN Br Het2 8017 O—(CH₂CH₂)—O CN Br Het2 8018 O—(CH₂CH₂CH₂)—O CN Br Het2 8019 S—(CH₂CH₂)—S CN Br Het2 8020 S—(CH₂CH₂CH₂)—S CN Br Het2 8021 —(CH₂)₄— CN Br Het2 8022 —(CH₂)₅— CN Br Het2 8023 H H F Br Het2 8024 CH₃ CH₃ F Br Het2 8025 CH₂CH₃ CH₂CH₃ F Br Het2 8026 CH₂CH₂CH₃ CH₂CH₂CH₃ F Br Het2 8027 OCH₃ OCH₃ F Br Het2 8028 OCH₂CH₃ OCH₂CH₃ F Br Het2 8029 OCH₂CH₂CH₃ OCH₂CH₂CH₃ F Br Het2 8030 SCH₃ SCH₃ F Br Het2 8031 SCH₂CH₃ SCH₂CH₃ F Br Het2 8032 N(CH₃)₂ N(CH₃)₂ F Br Het2 8033 N(CH₂CH₃)₂ N(CH₂CH₃)₂ F Br Het2 8034 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) F Br Het2 8035 O—(CH₂CH₂)—O F Br Het2 8036 O—(CH₂CH₂CH₂)—O F Br Het2 8037 S—(CH₂CH₂)—S F Br Het2 8038 S—(CH₂CH₂CH₂)—S F Br Het2 8039 —(CH₂)₄— F Br Het2 8040 —(CH₂)₅— F Br Het2 8041 H H Cl Br Het2 8042 CH₃ CH₃ Cl Br Het2 8043 CH₂CH₃ CH₂CH₃ Cl Br Het2 8044 CH₂CH₂CH₃ CH₂CH₂CH₃ Cl Br Het2 8045 OCH₃ OCH₃ Cl Br Het2 8046 OCH₂CH₃ OCH₂CH₃ Cl Br Het2 8047 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Cl Br Het2 8048 SCH₃ SCH₃ Cl Br Het2 8049 SCH₂CH₃ SCH₂CH₃ Cl Br Het2 8050 N(CH₃)₂ N(CH₃)₂ Cl Br Het2 8051 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Cl Br Het2 8052 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Cl Br Het2 8053 O—(CH₂CH₂)—O Cl Br Het2 8054 O—(CH₂CH₂CH₂)—O Cl Br Het2 8055 S—(CH₂CH₂)—S Cl Br Het2 8056 S—(CH₂CH₂CH₂)—S Cl Br Het2 8057 —(CH₂)₄— Cl Br Het2 8058 —(CH₂)₅— Cl Br Het2 8059 H H Br Br Het2 8060 CH₃ CH₃ Br Br Het2 8061 CH₂CH₃ CH₂CH₃ Br Br Het2 8062 CH₂CH₂CH₃ CH₂CH₂CH₃ Br Br Het2 8063 OCH₃ OCH₃ Br Br Het2 8064 OCH₂CH₃ OCH₂CH₃ Br Br Het2 8065 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Br Br Het2 8066 SCH₃ SCH₃ Br Br Het2 8067 SCH₂CH₃ SCH₂CH₃ Br Br Het2 8068 N(CH₃)₂ N(CH₃)₂ Br Br Het2 8069 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Br Br Het2 8070 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Br Br Het2 8071 O—(CH₂CH₂)—O Br Br Het2 8072 O—(CH₂CH₂CH₂)—O Br Br Het2 8073 S—(CH₂CH₂)—S Br Br Het2 8074 S—(CH₂CH₂CH₂)—S Br Br Het2 8075 —(CH₂)₄— Br Br Het2 8076 —(CH₂)₅— Br Br Het2 8077 H H CH₃ Br Het2 8078 CH₃ CH₃ CH₃ Br Het2 8079 CH₂CH₃ CH₂CH₃ CH₃ Br Het2 8080 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₃ Br Het2 8081 OCH₃ OCH₃ CH₃ Br Het2 8082 OCH₂CH₃ OCH₂CH₃ CH₃ Br Het2 8083 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₃ Br Het2 8084 SCH₃ SCH₃ CH₃ Br Het2 8085 SCH₂CH₃ SCH₂CH₃ CH₃ Br Het2 8086 N(CH₃)₂ N(CH₃)₂ CH₃ Br Het2 8087 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₃ Br Het2 8088 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₃ Br Het2 8089 O—(CH₂CH₂)—O CH₃ Br Het2 8090 O—(CH₂CH₂CH₂)—O CH₃ Br Het2 8091 S—(CH₂CH₂)—S CH₃ Br Het2 8092 S—(CH₂CH₂CH₂)—S CH₃ Br Het2 8093 —(CH₂)₄— CH₃ Br Het2 8094 —(CH₂)₅— CH₃ Br Het2 8095 H H CH₂CH₃ Br Het2 8096 CH₃ CH₃ CH₂CH₃ Br Het2 8097 CH₂CH₃ CH₂CH₃ CH₂CH₃ Br Het2 8098 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₂CH₃ Br Het2 8099 OCH₃ OCH₃ CH₂CH₃ Br Het2 8100 OCH₂CH₃ OCH₂CH₃ CH₂CH₃ Br Het2 8101 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₂CH₃ Br Het2 8102 SCH₃ SCH₃ CH₂CH₃ Br Het2 8103 SCH₂CH₃ SCH₂CH₃ CH₂CH₃ Br Het2 8104 N(CH₃)₂ N(CH₃)₂ CH₂CH₃ Br Het2 8105 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₂CH₃ Br Het2 8106 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₂CH₃ Br Het2 8107 O—(CH₂CH₂)—O CH₂CH₃ Br Het2 8108 O—(CH₂CH₂CH₂)—O CH₂CH₃ Br Het2 8109 S—(CH₂CH₂)—S CH₂CH₃ Br Het2 8110 S—(CH₂CH₂CH₂)—S CH₂CH₃ Br Het2 8111 —(CH₂)₄— CH₂CH₃ Br Het2 8112 —(CH₂)₅— CH₂CH₃ Br Het2 8113 H H CF₃ Br Het2 8114 CH₃ CH₃ CF₃ Br Het2 8115 CH₂CH₃ CH₂CH₃ CF₃ Br Het2 8116 CH₂CH₂CH₃ CH₂CH₂CH₃ CF₃ Br Het2 8117 OCH₃ OCH₃ CF₃ Br Het2 8118 OCH₂CH₃ OCH₂CH₃ CF₃ Br Het2 8119 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CF₃ Br Het2 8120 SCH₃ SCH₃ CF₃ Br Het2 8121 SCH₂CH₃ SCH₂CH₃ CF₃ Br Het2 8122 N(CH₃)₂ N(CH₃)₂ CF₃ Br Het2 8123 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CF₃ Br Het2 8124 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CF₃ Br Het2 8125 O—(CH₂CH₂)—O CF₃ Br Het2 8126 O—(CH₂CH₂CH₂)—O CF₃ Br Het2 8127 S—(CH₂CH₂)—S CF₃ Br Het2 8128 S—(CH₂CH₂CH₂)—S CF₃ Br Het2 8129 —(CH₂)₄— CF₃ Br Het2 8130 —(CH₂)₅— CF₃ Br Het2 8131 H H OCH₃ Br Het2 8132 CH₃ CH₃ OCH₃ Br Het2 8133 CH₂CH₃ CH₂CH₃ OCH₃ Br Het2 8134 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₃ Br Het2 8135 OCH₃ OCH₃ OCH₃ Br Het2 8136 OCH₂CH₃ OCH₂CH₃ OCH₃ Br Het2 8137 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₃ Br Het2 8138 SCH₃ SCH₃ OCH₃ Br Het2 8139 SCH₂CH₃ SCH₂CH₃ OCH₃ Br Het2 8140 N(CH₃)₂ N(CH₃)₂ OCH₃ Br Het2 8141 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₃ Br Het2 8142 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₃ Br Het2 8143 O—(CH₂CH₂)—O OCH₃ Br Het2 8144 O—(CH₂CH₂CH₂)—O OCH₃ Br Het2 8145 S—(CH₂CH₂)—S OCH₃ Br Het2 8146 S—(CH₂CH₂CH₂)—S OCH₃ Br Het2 8147 —(CH₂)₄— OCH₃ Br Het2 8148 —(CH₂)₅— OCH₃ Br Het2 8149 H H OCH₂CH₃ Br Het2 8150 CH₃ CH₃ OCH₂CH₃ Br Het2 8151 CH₂CH₃ CH₂CH₃ OCH₂CH₃ Br Het2 8152 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₂CH₃ Br Het2 8153 OCH₃ OCH₃ OCH₂CH₃ Br Het2 8154 OCH₂CH₃ OCH₂CH₃ OCH₂CH₃ Br Het2 8155 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₂CH₃ Br Het2 8156 SCH₃ SCH₃ OCH₂CH₃ Br Het2 8157 SCH₂CH₃ SCH₂CH₃ OCH₂CH₃ Br Het2 8158 N(CH₃)₂ N(CH₃)₂ OCH₂CH₃ Br Het2 8159 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₂CH₃ Br Het2 8160 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₂CH₃ Br Het2 8161 O—(CH₂CH₂)—O OCH₂CH₃ Br Het2 8162 O—(CH₂CH₂CH₂)—O OCH₂CH₃ Br Het2 8163 S—(CH₂CH₂)—S OCH₂CH₃ Br Het2 8164 S—(CH₂CH₂CH₂)—S OCH₂CH₃ Br Het2 8165 —(CH₂)₄— OCH₂CH₃ Br Het2 8166 —(CH₂)₅— OCH₂CH₃ Br Het2 8167 H H SCH₃ Br Het2 8168 CH₃ CH₃ SCH₃ Br Het2 8169 CH₂CH₃ CH₂CH₃ SCH₃ Br Het2 8170 CH₂CH₂CH₃ CH₂CH₂CH₃ SCH₃ Br Het2 8171 OCH₃ OCH₃ SCH₃ Br Het2 8172 OCH₂CH₃ OCH₂CH₃ SCH₃ Br Het2 8173 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SCH₃ Br Het2 8174 SCH₃ SCH₃ SCH₃ Br Het2 8175 SCH₂CH₃ SCH₂CH₃ SCH₃ Br Het2 8176 N(CH₃)₂ N(CH₃)₂ SCH₃ Br Het2 8177 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SCH₃ Br Het2 8178 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SCH₃ Br Het2 8179 O—(CH₂CH₂)—O SCH₃ Br Het2 8180 O—(CH₂CH₂CH₂)—O SCH₃ Br Het2 8181 S—(CH₂CH₂)—S SCH₃ Br Het2 8182 S—(CH₂CH₂CH₂)—S SCH₃ Br Het2 8183 —(CH₂)₄— SCH₃ Br Het2 8184 —(CH₂)₅— SCH₃ Br Het2 8185 H H SO₂CH₃ Br Het2 8186 CH₃ CH₃ SO₂CH₃ Br Het2 8187 CH₂CH₃ CH₂CH₃ SO₂CH₃ Br Het2 8188 CH₂CH₂CH₃ CH₂CH₂CH₃ SO₂CH₃ Br Het2 8189 OCH₃ OCH₃ SO₂CH₃ Br Het2 8190 OCH₂CH₃ OCH₂CH₃ SO₂CH₃ Br Het2 8191 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SO₂CH₃ Br Het2 8192 SCH₃ SCH₃ SO₂CH₃ Br Het2 8193 SCH₂CH₃ SCH₂CH₃ SO₂CH₃ Br Het2 8194 N(CH₃)₂ N(CH₃)₂ SO₂CH₃ Br Het2 8195 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SO₂CH₃ Br Het2 8196 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SO₂CH₃ Br Het2 8197 O—(CH₂CH₂)—O SO₂CH₃ Br Het2 8198 O—(CH₂CH₂CH₂)—O SO₂CH₃ Br Het2 8199 S—(CH₂CH₂)—S SO₂CH₃ Br Het2 8200 S—(CH₂CH₂CH₂)—S SO₂CH₃ Br Het2 8201 —(CH₂)₄— SO₂CH₃ Br Het2 8202 —(CH₂)₅— SO₂CH₃ Br Het2 8203 H H PO(OCH₃)₂ Br Het2 8204 CH₃ CH₃ PO(OCH₃)₂ Br Het2 8205 CH₂CH₃ CH₂CH₃ PO(OCH₃)₂ Br Het2 8206 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₃)₂ Br Het2 8207 OCH₃ OCH₃ PO(OCH₃)₂ Br Het2 8208 OCH₂CH₃ OCH₂CH₃ PO(OCH₃)₂ Br Het2 8209 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₃)₂ Br Het2 8210 SCH₃ SCH₃ PO(OCH₃)₂ Br Het2 8211 SCH₂CH₃ SCH₂CH₃ PO(OCH₃)₂ Br Het2 8212 N(CH₃)₂ N(CH₃)₂ PO(OCH₃)₂ Br Het2 8213 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₃)₂ Br Het2 8214 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₃)₂ Br Het2 8215 O—(CH₂CH₂)—O PO(OCH₃)₂ Br Het2 8216 O—(CH₂CH₂CH₂)—O PO(OCH₃)₂ Br Het2 8217 S—(CH₂CH₂)—S PO(OCH₃)₂ Br Het2 8218 S—(CH₂CH₂CH₂)—S PO(OCH₃)₂ Br Het2 8219 —(CH₂)₄— PO(OCH₃)₂ Br Het2 8220 —(CH₂)₅— PO(OCH₃)₂ Br Het2 8221 H H PO(OCH₂CH₃)₂ Br Het2 8222 CH₃ CH₃ PO(OCH₂CH₃)₂ Br Het2 8223 CH₂CH₃ CH₂CH₃ PO(OCH₂CH₃)₂ Br Het2 8224 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₂CH₃)₂ Br Het2 8225 OCH₃ OCH₃ PO(OCH₂CH₃)₂ Br Het2 8226 OCH₂CH₃ OCH₂CH₃ PO(OCH₂CH₃)₂ Br Het2 8227 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₂CH₃)₂ Br Het2 8228 SCH₃ SCH₃ PO(OCH₂CH₃)₂ Br Het2 8229 SCH₂CH₃ SCH₂CH₃ PO(OCH₂CH₃)₂ Br Het2 8230 N(CH₃)₂ N(CH₃)₂ PO(OCH₂CH₃)₂ Br Het2 8231 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₂CH₃)₂ Br Het2 8232 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₂CH₃)₂ Br Het2 8233 O—(CH₂CH₂)—O PO(OCH₂CH₃)₂ Br Het2 8234 O—(CH₂CH₂CH₂)—O PO(OCH₂CH₃)₂ Br Het2 8235 S—(CH₂CH₂)—S PO(OCH₂CH₃)₂ Br Het2 8236 S—(CH₂CH₂CH₂)—S PO(OCH₂CH₃)₂ Br Het2 8237 —(CH₂)₄— PO(OCH₂CH₃)₂ Br Het2 8238 —(CH₂)₅— PO(OCH₂CH₃)₂ Br Het2 8239 H H PO(CH₃)₂ Br Het2 8240 CH₃ CH₃ PO(CH₃)₂ Br Het2 8241 CH₂CH₃ CH₂CH₃ PO(CH₃)₂ Br Het2 8242 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₃)₂ Br Het2 8243 OCH₃ OCH₃ PO(CH₃)₂ Br Het2 8244 OCH₂CH₃ OCH₂CH₃ PO(CH₃)₂ Br Het2 8245 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₃)₂ Br Het2 8246 SCH₃ SCH₃ PO(CH₃)₂ Br Het2 8247 SCH₂CH₃ SCH₂CH₃ PO(CH₃)₂ Br Het2 8248 N(CH₃)₂ N(CH₃)₂ PO(CH₃)₂ Br Het2 8249 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₃)₂ Br Het2 8250 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₃)₂ Br Het2 8251 O—(CH₂CH₂)—O PO(CH₃)₂ Br Het2 8252 O—(CH₂CH₂CH₂)—O PO(CH₃)₂ Br Het2 8253 S—(CH₂CH₂)—S PO(CH₃)₂ Br Het2 8254 S—(CH₂CH₂CH₂)—S PO(CH₃)₂ Br Het2 8255 —(CH₂)₄— PO(CH₃)₂ Br Het2 8256 —(CH₂)₅— PO(CH₃)₂ Br Het2 8257 H H PC(CH₂CH₃)₂ Br Het2 8258 CH₃ CH₃ PC(CH₂CH₃)₂ Br Het2 8259 CH₂CH₃ CH₂CH₃ PC(CH₂CH₃)₂ Br Het2 8260 CH₂CH₂CH₃ CH₂CH₂CH₃ PC(CH₂CH₃)₂ Br Het2 8261 OCH₃ OCH₃ PC(CH₂CH₃)₂ Br Het2 8262 OCH₂CH₃ OCH₂CH₃ PC(CH₂CH₃)₂ Br Het2 8263 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PC(CH₂CH₃)₂ Br Het2 8264 SCH₃ SCH₃ PC(CH₂CH₃)₂ Br Het2 8265 SCH₂CH₃ SCH₂CH₃ PC(CH₂CH₃)₂ Br Het2 8266 N(CH₃)₂ N(CH₃)₂ PC(CH₂CH₃)₂ Br Het2 8267 N(CH_(2CH) ₃)₂ N(CH₂CH₃)₂ PC(CH₂CH₃)₂ Br Het2 8268 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PC(CH₂CH₃)₂ Br Het2 8269 O—(CH₂CH₂)—O PC(CH₂CH₃)₂ Br Het2 8270 O—(CH₂CH₂CH₂)—O PC(CH₂CH₃)₂ Br Het2 8271 S—(CH₂CH₂)—S PC(CH₂CH₃)₂ Br Het2 8272 S—(CH₂CH₂CH₂)—S PC(CH₂CH₃)₂ Br Het2 8273 —(CH₂)₄— PC(CH₂CH₃)₂ Br Het2 8274 —(CH₂)₅— PC(CH₂CH₃)₂ Br Het2 8275 H H H Br Het3 8276 CH₃ CH₃ H Br Het3 8277 CH₂CH₃ CH₂CH₃ H Br Het3 8278 CH₂CH₂CH₃ CH₂CH₂CH₃ H Br Het3 8279 OCH₃ OCH₃ H Br Het3 8280 OCH₂CH₃ OCH₂CH₃ H Br Het3 8281 OCH₂CH₂CH₃ OCH₂CH₂CH₃ H Br Het3 8282 SCH₃ SCH₃ H Br Het3 8283 SCH₂CH₃ SCH₂CH₃ H Br Het3 8284 N(CH₃)₂ N(CH₃)₂ H Br Het3 8285 N(CH₂CH₃)₂ N(CH₂CH₃)₂ H Br Het3 8286 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) H Br Het3 8287 O—(CH₂CH₂)—O H Br Het3 8288 O—(CH₂CH₂CH₂)—O H Br Het3 8289 S—(CH₂CH₂)—S H Br Het3 8290 S—(CH₂CH₂CH₂)—S H Br Het3 8291 —(CH₂)₄— H Br Het3 8292 —(CH₂)₅— H Br Het3 8293 H H NO₂ Br Het3 8294 CH₃ CH₃ NO₂ Br Het3 8295 CH₂CH₃ CH₂CH₃ NO₂ Br Het3 8296 CH₂CH₂CH₃ CH₂CH₂CH₃ NO₂ Br Het3 8297 OCH₃ OCH₃ NO₂ Br Het3 8298 OCH₂CH₃ OCH₂CH₃ NO₂ Br Het3 8299 OCH₂CH₂CH₃ OCH₂CH₂CH₃ NO₂ Br Het3 8300 SCH₃ SCH₃ NO₂ Br Het3 8301 SCH₂CH₃ SCH₂CH₃ NO₂ Br Het3 8302 N(CH₃)₂ N(CH₃)₂ NO₂ Br Het3 8303 N(CH₂CH₃)₂ N(CH₂CH₃)₂ NO₂ Br Het3 8304 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) NO₂ Br Het3 8305 O—(CH₂CH₂)—O NO₂ Br Het3 8306 O—(CH₂CH₂CH₂)—O NO₂ Br Het3 8307 S—(CH₂CH₂)—S NO₂ Br Het3 8308 S—(CH₂CH₂CH₂)—S NO₂ Br Het3 8309 —(CH₂)₄— NO₂ Br Het3 8310 —(CH₂)₅— NO₂ Br Het3 8311 H H CN Br Het3 8312 CH₃ CH₃ CN Br Het3 8313 CH₂CH₃ CH₂CH₃ CN Br Het3 8314 CH₂CH₂CH₃ CH₂CH₂CH₃ CN Br Het3 8315 OCH₃ OCH₃ CN Br Het3 8316 OCH₂CH₃ OCH₂CH₃ CN Br Het3 8317 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CN Br Het3 8318 SCH₃ SCH₃ CN Br Het3 8319 SCH₂CH₃ SCH₂CH₃ CN Br Het3 8320 N(CH₃)₂ N(CH₃)₂ CN Br Het3 8321 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CN Br Het3 8322 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CN Br Het3 8323 O—(CH₂CH₂)—O CN Br Het3 8324 O—(CH₂CH₂CH₂)—O CN Br Het3 8325 S—(CH₂CH₂)—S CN Br Het3 8326 S—(CH₂CH₂CH₂)—S CN Br Het3 8327 —(CH₂)₄— CN Br Het3 8328 —(CH₂)₅— CN Br Het3 8329 H H F Br Het3 8330 CH₃ CH₃ F Br Het3 8331 CH₂CH₃ CH₂CH₃ F Br Het3 8332 CH₂CH₂CH₃ CH₂CH₂CH₃ F Br Het3 8333 OCH₃ OCH₃ F Br Het3 8334 OCH₂CH₃ OCH₂CH₃ F Br Het3 8335 OCH₂CH₂CH₃ OCH₂CH₂CH₃ F Br Het3 8336 SCH₃ SCH₃ F Br Het3 8337 SCH₂CH₃ SCH₂CH₃ F Br Het3 8338 N(CH₃)₂ N(CH₃)₂ F Br Het3 8339 N(CH₂CH₃)₂ N(CH₂CH₃)₂ F Br Het3 8340 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) F Br Het3 8341 O—(CH₂CH₂)—O F Br Het3 8342 O—(CH₂CH₂CH₂)—O F Br Het3 8343 S—(CH₂CH₂)—S F Br Het3 8344 S—(CH₂CH₂CH₂)—S F Br Het3 8345 —(CH₂)₄— F Br Het3 8346 —(CH₂)₅— F Br Het3 8347 H H Cl Br Het3 8348 CH₃ CH₃ Cl Br Het3 8349 CH₂CH₃ CH₂CH₃ Cl Br Het3 8350 CH₂CH₂CH₃ CH₂CH₂CH₃ Cl Br Het3 8351 OCH₃ OCH₃ Cl Br Het3 8352 OCH₂CH₃ OCH₂CH₃ Cl Br Het3 8353 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Cl Br Het3 8354 SCH₃ SCH₃ Cl Br Het3 8355 SCH₂CH₃ SCH₂CH₃ Cl Br Het3 8356 N(CH₃)₂ N(CH₃)₂ Cl Br Het3 8357 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Cl Br Het3 8358 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Cl Br Het3 8359 O—(CH₂CH₂)—O Cl Br Het3 8360 O—(CH₂CH₂CH₂)—O Cl Br Het3 8361 S—(CH₂CH₂)—S Cl Br Het3 8362 S—(CH₂CH₂CH₂)—S Cl Br Het3 8363 —(CH₂)₄— Cl Br Het3 8364 —(CH₂)₅— Cl Br Het3 8365 H H Br Br Het3 8366 CH₃ CH₃ Br Br Het3 8367 CH₂CH₃ CH₂CH₃ Br Br Het3 8368 CH₂CH₂CH₃ CH₂CH₂CH₃ Br Br Het3 8369 OCH₃ OCH₃ Br Br Het3 8370 OCH₂CH₃ OCH₂CH₃ Br Br Het3 8371 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Br Br Het3 8372 SCH₃ SCH₃ Br Br Het3 8373 SCH₂CH₃ SCH₂CH₃ Br Br Het3 8374 N(CH₃)₂ N(CH₃)₂ Br Br Het3 8375 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Br Br Het3 8376 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Br Br Het3 8377 O—(CH₂CH₂)—O Br Br Het3 8378 O—(CH₂CH₂CH₂)—O Br Br Het3 8379 S—(CH₂CH₂)—S Br Br Het3 8380 S—(CH₂CH₂CH₂)—S Br Br Het3 8381 —(CH₂)₄— Br Br Het3 8382 —(CH₂)₅— Br Br Het3 8383 H H CH₃ Br Het3 8384 CH₃ CH₃ CH₃ Br Het3 8385 CH₂CH₃ CH₂CH₃ CH₃ Br Het3 8386 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₃ Br Het3 8387 OCH₃ OCH₃ CH₃ Br Het3 8388 OCH₂CH₃ OCH₂CH₃ CH₃ Br Het3 8389 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₃ Br Het3 8390 SCH₃ SCH₃ CH₃ Br Het3 8391 SCH₂CH₃ SCH₂CH₃ CH₃ Br Het3 8392 N(CH₃)₂ N(CH₃)₂ CH₃ Br Het3 8393 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₃ Br Het3 8394 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₃ Br Het3 8395 O—(CH₂CH₂)—O CH₃ Br Het3 8396 O—(CH₂CH₂CH₂)—O CH₃ Br Het3 8397 S—(CH₂CH₂)—S CH₃ Br Het3 8398 S—(CH₂CH₂CH₂)—S CH₃ Br Het3 8399 —(CH₂)₄— CH₃ Br Het3 8400 —(CH₂)₅— CH₃ Br Het3 8401 H H CH₂CH₃ Br Het3 8402 CH₃ CH₃ CH₂CH₃ Br Het3 8403 CH₂CH₃ CH₂CH₃ CH₂CH₃ Br Het3 8404 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₂CH₃ Br Het3 8405 OCH₃ OCH₃ CH₂CH₃ Br Het3 8406 OCH₂CH₃ OCH₂CH₃ CH₂CH₃ Br Het3 8407 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₂CH₃ Br Het3 8408 SCH₃ SCH₃ CH₂CH₃ Br Het3 8409 SCH₂CH₃ SCH₂CH₃ CH₂CH₃ Br Het3 8410 N(CH₃)₂ N(CH₃)₂ CH₂CH₃ Br Het3 8411 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₂CH₃ Br Het3 8412 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₂CH₃ Br Het3 8413 O—(CH₂CH₂)—O CH₂CH₃ Br Het3 8414 O—(CH₂CH₂CH₂)—O CH₂CH₃ Br Het3 8415 S—(CH₂CH₂)—S CH₂CH₃ Br Het3 8416 S—(CH₂CH₂CH₂)—S CH₂CH₃ Br Het3 8417 —(CH₂)₄— CH₂CH₃ Br Het3 8418 —(CH₂)₅— CH₂CH₃ Br Het3 8419 H H CF₃ Br Het3 8420 CH₃ CH₃ CF₃ Br Het3 8421 CH₂CH₃ CH₂CH₃ CF₃ Br Het3 8422 CH₂CH₂CH₃ CH₂CH₂CH₃ CF₃ Br Het3 8423 OCH₃ OCH₃ CF₃ Br Het3 8424 OCH₂CH₃ OCH₂CH₃ CF₃ Br Het3 8425 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CF₃ Br Het3 8426 SCH₃ SCH₃ CF₃ Br Het3 8427 SCH₂CH₃ SCH₂CH₃ CF₃ Br Het3 8428 N(CH₃)₂ N(CH₃)₂ CF₃ Br Het3 8429 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CF₃ Br Het3 8430 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CF₃ Br Het3 8431 O—(CH₂CH₂)—O CF₃ Br Het3 8432 O—(CH₂CH₂CH₂)—O CF₃ Br Het3 8433 S—(CH₂CH₂)—S CF₃ Br Het3 8434 S—(CH₂CH₂CH₂)—S CF₃ Br Het3 8435 —(CH₂)₄— CF₃ Br Het3 8436 —(CH₂)₅— CF₃ Br Het3 8437 H H OCH₃ Br Het3 8438 CH₃ CH₃ OCH₃ Br Het3 8439 CH₂CH₃ CH₂CH₃ OCH₃ Br Het3 8440 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₃ Br Het3 8441 OCH₃ OCH₃ OCH₃ Br Het3 8442 OCH₂CH₃ OCH₂CH₃ OCH₃ Br Het3 8443 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₃ Br Het3 8444 SCH₃ SCH₃ OCH₃ Br Het3 8445 SCH₂CH₃ SCH₂CH₃ OCH₃ Br Het3 8446 N(CH₃)₂ N(CH₃)₂ OCH₃ Br Het3 8447 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₃ Br Het3 8448 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₃ Br Het3 8449 O—(CH₂CH₂)—O OCH₃ Br Het3 8450 O—(CH₂CH₂CH₂)—O OCH₃ Br Het3 8451 S—(CH₂CH₂)—S OCH₃ Br Het3 8452 S—(CH₂CH₂CH₂)—S OCH₃ Br Het3 8453 —(CH₂)₄— OCH₃ Br Het3 8454 —(CH₂)₅— OCH₃ Br Het3 8455 H H OCH₂CH₃ Br Het3 8456 CH₃ CH₃ OCH₂CH₃ Br Het3 8457 CH₂CH₃ CH₂CH₃ OCH₂CH₃ Br Het3 8458 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₂CH₃ Br Het3 8459 OCH₃ OCH₃ OCH₂CH₃ Br Het3 8460 OCH₂CH₃ OCH₂CH₃ OCH₂CH₃ Br Het3 8461 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₂CH₃ Br Het3 8462 SCH₃ SCH₃ OCH₂CH₃ Br Het3 8463 SCH₂CH₃ SCH₂CH₃ OCH₂CH₃ Br Het3 8464 N(CH₃)₂ N(CH₃)₂ OCH₂CH₃ Br Het3 8465 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₂CH₃ Br Het3 8466 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₂CH₃ Br Het3 8467 O—(CH₂CH₂)—O OCH₂CH₃ Br Het3 8468 O—(CH₂CH₂CH₂)—O OCH₂CH₃ Br Het3 8469 S—(CH₂CH₂)—S OCH₂CH₃ Br Het3 8470 S—(CH₂CH₂CH₂)—S OCH₂CH₃ Br Het3 8471 —(CH₂)₄— OCH₂CH₃ Br Het3 8472 —(CH₂)₅— OCH₂CH₃ Br Het3 8473 H H SCH₃ Br Het3 8474 CH₃ CH₃ SCH₃ Br Het3 8475 CH₂CH₃ CH₂CH₃ SCH₃ Br Het3 8476 CH₂CH₂CH₃ CH₂CH₂CH₃ SCH₃ Br Het3 8477 OCH₃ OCH₃ SCH₃ Br Het3 8478 OCH₂CH₃ OCH₂CH₃ SCH₃ Br Het3 8479 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SCH₃ Br Het3 8480 SCH₃ SCH₃ SCH₃ Br Het3 8481 SCH₂CH₃ SCH₂CH₃ SCH₃ Br Het3 8482 N(CH₃)₂ N(CH₃)₂ SCH₃ Br Het3 8483 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SCH₃ Br Het3 8484 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SCH₃ Br Het3 8485 O—(CH₂CH₂)—O SCH₃ Br Het3 8486 O—(CH₂CH₂CH₂)—O SCH₃ Br Het3 8487 S—(CH₂CH₂)—S SCH₃ Br Het3 8488 S—(CH₂CH₂CH₂)—S SCH₃ Br Het3 8489 —(CH₂)₄— SCH₃ Br Het3 8490 —(CH₂)₅— SCH₃ Br Het3 8491 H H SO₂CH₃ Br Het3 8492 CH₃ CH₃ SO₂CH₃ Br Het3 8493 CH₂CH₃ CH₂CH₃ SO₂CH₃ Br Het3 8494 CH₂CH₂CH₃ CH₂CH₂CH₃ SO₂CH₃ Br Het3 8495 OCH₃ OCH₃ SO₂CH₃ Br Het3 8496 OCH₂CH₃ OCH₂CH₃ SO₂CH₃ Br Het3 8497 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SO₂CH₃ Br Het3 8498 SCH₃ SCH₃ SO₂CH₃ Br Het3 8499 SCH₂CH₃ SCH₂CH₃ SO₂CH₃ Br Het3 8500 N(CH₃)₂ N(CH₃)₂ SO₂CH₃ Br Het3 8501 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SO₂CH₃ Br Het3 8502 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SO₂CH₃ Br Het3 8503 O—(CH₂CH₂)—O SO₂CH₃ Br Het3 8504 O—(CH₂CH₂CH₂)—O SO₂CH₃ Br Het3 8505 S—(CH₂CH₂)—S SO₂CH₃ Br Het3 8506 S—(CH₂CH₂CH₂)—S SO₂CH₃ Br Het3 8507 —(CH₂)₄— SO₂CH₃ Br Het3 8508 —(CH₂)₅— SO₂CH₃ Br Het3 8509 H H PO(OCH₃)₂ Br Het3 8510 CH₃ CH₃ PO(OCH₃)₂ Br Het3 8511 CH₂CH₃ CH₂CH₃ PO(OCH₃)₂ Br Het3 8512 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₃)₂ Br Het3 8513 OCH₃ OCH₃ PO(OCH₃)₂ Br Het3 8514 OCH₂CH₃ OCH₂CH₃ PO(OCH₃)₂ Br Het3 8515 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₃)₂ Br Het3 8516 SCH₃ SCH₃ PO(OCH₃)₂ Br Het3 8517 SCH₂CH₃ SCH₂CH₃ PO(OCH₃)₂ Br Het3 8518 N(CH₃)₂ N(CH₃)₂ PO(OCH₃)₂ Br Het3 8519 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₃)₂ Br Het3 8520 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₃)₂ Br Het3 8521 O—(CH₂CH₂)—O PO(OCH₃)₂ Br Het3 8522 O—(CH₂CH₂CH₂)—O PO(OCH₃)₂ Br Het3 8523 S—(CH₂CH₂)—S PO(OCH₃)₂ Br Het3 8524 S—(CH₂CH₂CH₂)—S PO(OCH₃)₂ Br Het3 8525 —(CH₂)₄— PO(OCH₃)₂ Br Het3 8526 —(CH₂)₅— PO(OCH₃)₂ Br Het3 8527 H H PO(OCH₂CH₃)₂ Br Het3 8528 CH₃ CH₃ PO(OCH₂CH₃)₂ Br Het3 8529 CH₂CH₃ CH₂CH₃ PO(OCH₂CH₃)₂ Br Het3 8530 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₂CH₃)₂ Br Het3 8531 OCH₃ OCH₃ PO(OCH₂CH₃)₂ Br Het3 8532 OCH₂CH₃ OCH₂CH₃ PO(OCH₂CH₃)₂ Br Het3 8533 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₂CH₃)₂ Br Het3 8534 SCH₃ SCH₃ PO(OCH₂CH₃)₂ Br Het3 8535 SCH₂CH₃ SCH₂CH₃ PO(OCH₂CH₃)₂ Br Het3 8536 N(CH₃)₂ N(CH₃)₂ PO(OCH₂CH₃)₂ Br Het3 8537 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₂CH₃)₂ Br Het3 8538 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₂CH₃)₂ Br Het3 8539 O—(CH₂CH₂)—O PO(OCH₂CH₃)₂ Br Het3 8540 O—(CH₂CH₂CH₂)—O PO(OCH₂CH₃)₂ Br Het3 8541 S—(CH₂CH₂)—S PO(OCH₂CH₃)₂ Br Het3 8542 S—(CH₂CH₂CH₂)—S PO(OCH₂CH₃)₂ Br Het3 8543 —(CH₂)₄— PO(OCH₂CH₃)₂ Br Het3 8544 —(CH₂)₅— PO(OCH₂CH₃)₂ Br Het3 8545 H H PO(CH₃)₂ Br Het3 8546 CH₃ CH₃ PO(CH₃)₂ Br Het3 8547 CH₂CH₃ CH₂CH₃ PO(CH₃)₂ Br Het3 8548 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₃)₂ Br Het3 8549 OCH₃ OCH₃ PO(CH₃)₂ Br Het3 8550 OCH₂CH₃ OCH₂CH₃ PO(CH₃)₂ Br Het3 8551 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₃)₂ Br Het3 8552 SCH₃ SCH₃ PO(CH₃)₂ Br Het3 8553 SCH₂CH₃ SCH₂CH₃ PO(CH₃)₂ Br Het3 8554 N(CH₃)₂ N(CH₃)₂ PO(CH₃)₂ Br Het3 8555 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₃)₂ Br Het3 8556 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₃)₂ Br Het3 8557 O—(CH₂CH₂)—O PO(CH₃)₂ Br Het3 8558 O—(CH₂CH₂CH₂)—O PO(CH₃)₂ Br Het3 8559 S—(CH₂CH₂)—S PO(CH₃)₂ Br Het3 8560 S—(CH₂CH₂CH₂)—S PO(CH₃)₂ Br Het3 8561 —(CH₂)₄— PO(CH₃)₂ Br Het3 8562 —(CH₂)₅— PO(CH₃)₂ Br Het3 8563 H H PC(CH₂CH₃)₂ Br Het3 8564 CH₃ CH₃ PC(CH₂CH₃)₂ Br Het3 8565 CH₂CH₃ CH₂CH₃ PC(CH₂CH₃)₂ Br Het3 8566 CH₂CH₂CH₃ CH₂CH₂CH₃ PC(CH₂CH₃)₂ Br Het3 8567 OCH₃ OCH₃ PC(CH₂CH₃)₂ Br Het3 8568 OCH₂CH₃ OCH₂CH₃ PC(CH₂CH₃)₂ Br Het3 8569 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PC(CH₂CH₃)₂ Br Het3 8570 SCH₃ SCH₃ PC(CH₂CH₃)₂ Br Het3 8571 SCH₂CH₃ SCH₂CH₃ PC(CH₂CH₃)₂ Br Het3 8572 N(CH₃)₂ N(CH₃)₂ PC(CH₂CH₃)₂ Br Het3 8573 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PC(CH₂CH₃)₂ Br Het3 8574 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PC(CH₂CH₃)₂ Br Het3 8575 O—(CH₂CH₂)—O PC(CH₂CH₃)₂ Br Het3 8576 O—(CH₂CH₂CH₂)—O PC(CH₂CH₃)₂ Br Het3 8577 S—(CH₂CH₂)—S PC(CH₂CH₃)₂ Br Het3 8578 S—(CH₂CH₂CH₂)—S PC(CH₂CH₃)₂ Br Het3 8579 —(CH₂)₄— PC(CH₂CH₃)₂ Br Het3 8580 —(CH₂)₅— PC(CH₂CH₃)₂ Br Het3

where:

Het1 is 1-methoxy-N-methylamino;

Het2 is 1-tetrahydropyrrolyl;

Het3 is 1-tetrahydroisoxazolyl.

Extraordinary preference is also given to the compounds I1a2 (≡I where X=O; R³ is attached in the 4-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 2-position; Q=Q¹; R⁷, R⁸, R⁹, R¹¹, R¹²=H and R¹⁰=CH₃), in particular to the compounds I1a2.n, where the variables R¹ to R⁴ and R⁶ are as defined in Table 1.

Extraordinary preference is also given to the compounds I1a3 (≡I where X=O; R³ is attached in the 4-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 2-position; Q=Q¹; R⁸, R⁹, R¹⁰, R¹¹, R¹²=H and R⁷=CH₃), in particular to the compounds I1a3.n, where the variables R¹ to R⁴ and R⁶ are as defined in Table 1.

Extraordinary preference is also given to the compounds I1a4 (≡I where X=O; R³ is attached in the 4-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 2-position; Q=Q¹; R⁷, R⁸, R¹¹, R¹²=H and R⁹, R¹⁰=CH₃), in particular to the compounds I1a4.n, where the variables R¹ to R⁴ and R⁶ are as defined in Table 1.

Extraordinary preference is also given to the compounds I1a5 (≡I where X=O; R³ is attached in the 4-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 2-position; Q=Q¹; R⁷, R⁸=CH₃ and R⁹, R¹⁰, R¹¹, R¹²=H), in particular to the compounds I1a5.n, where the variables R¹ to R⁴ and R⁶ are as defined in Table 1.

Extraordinary preference is also given to the compounds I1a6 (≡I where X=O; R³ is attached in the 4-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 2-position; Q=Q¹; R⁷, R⁸, R⁹, R¹⁰=H and R¹¹, R¹²=CH₃), in particular to the compounds I1a6.n, where the variables R¹ to R⁴ and R⁶ are as defined in Table 1.

Extraordinary preference is also given to the compounds I1a7 (≡I where X=O; R³ is attached in the 4-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 2-position; Q=Q¹; R⁷, R⁸, R¹¹, R¹²=H and R⁹ and R¹⁰ together with the carbon to which they are attached form a carbonyl group), in particular to the compounds I1a7.n, where the variables R¹ to R⁴ and R⁶ are as defined in Table 1.

Extraordinary preference is also given to the compounds I1a8 (≡I where X=O; R³ is attached in the 4-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 2-position; Q=Q¹; R⁷, R⁸, R¹¹, R¹²=CH₃ and R⁹ and R¹⁰ together with the carbon to which they are attached form a carbonyl group), in particular to the compounds I1a8.n, where the variables R¹ to R⁴ and R⁶ are as defined in Table 1.

Extraordinary preference is also given to the compounds I1a9 (≡I where X=O; R³ is attached in the 4-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 2-position; Q=Q¹; R⁷ and R¹¹ together form a —CH₂—CH₂— chain and R⁸, R⁹, R¹⁰, R¹²=H), in particular to the compounds I1a9.n, where the variables R¹ to R⁴ and R⁶ are as defined in Table 1.

Extraordinary preference is also given to the compounds I2a1 (≡I where X=O; R³ is attached in the 2-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 4-position; Q=Q¹; R⁷, R⁸, R⁹, R¹⁰, R¹¹, R¹²=H), in particular to the compounds I2a1.n, where the variables R¹ to R⁴ and R⁶ are as defined in Table 1.

Extraordinary preference is also given to the compounds I2a2 (≡I where X=O; R³ is attached in the 2-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 4-position; Q=Q¹; R⁷, R⁸, R⁹, R¹¹, R¹²=H and R¹⁰=CH₃), in particular to the compounds I2a2.n, where the variables R¹ to R⁴ and R⁶ are as defined in Table 1.

Extraordinary preference is also given to the compounds I2a3 (≡I where X=O; R³ is attached in the 2-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 4-position; Q=Q¹; R⁸, R⁹, R¹⁰, R¹¹, R¹²=H and R⁷=CH₃), in particular to the compounds I2a3.n, where the variables R¹ to R⁴ and R⁶ are as defined in Table 1.

Extraordinary preference is also given to the compounds I2a4 (≡I where X=O; R³ is attached in the 2-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 4-position; Q=Q¹; R⁷, R⁸, R¹¹, R¹²=H and R⁹, R¹⁰=CH₃), in particular to the compounds I2a4.n, where the variables R¹ to R⁴ and R⁶ are as defined in Table 1.

Extraordinary preference is also given to the compounds I2a5 (≡I where X=O; R³ is attached in the 2-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 4-position; Q=Q¹; R⁷, R⁸=CH₃, R⁹, R¹⁰, R¹¹, R¹²=H), in particular to the compounds I2a5.n, where the variables R¹ to R⁴ and R⁶ are as defined in Table 1.

Extraordinary preference is also given to the compounds I2a6 (≡I where X=O; R³ is attached in the 2-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 4-position; Q=Q¹; R⁷, R⁸, R⁹, R¹⁰=H and R¹¹, R¹²=CH₃), in particular to the compounds I2a6.n, where the variables R¹ to R⁴ and R⁶ are as defined in Table 1.

Extraordinary preference is also given to the compounds I2a7 (≡I where X=O; R³ is attached in the 2-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 4-position; Q=Q¹; R⁷, R⁸, R¹¹, R¹²=H and R⁹ and R¹⁰ together with the carbon to which they are attached form a carbonyl group), in particular to the compounds I2a7.n, where the variables R¹ to R⁴ and R⁶ are as defined in Table 1.

Extraordinary preference is also given to the compounds I2a8 (≡I where X=O; R³ is attached in the 2-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 4-position; Q=Q¹; R⁷, R⁸, R¹¹, R¹²=CH₃ and R⁹ and R¹⁰ together with the carbon to which they are attached form a carbonyl group), in particular to the compounds I2a8.n, where the variables R¹ to R⁴ and R⁶ are as defined in Table 1.

Extraordinary preference is also given to the compounds I2a9 (≡I where X=O; R³ is attached in the 2-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 4-position; Q=Q¹; R⁷ and R¹¹ together form a —CH₂—CH₂— chain and R⁸, R⁹, R¹⁰, R¹²=H), in particular to the compounds I2a9.n, where the variables R¹ to R⁴ and R⁶ are as defined in Table 1.

Extraordinary preference is also given to the compounds I1b1 (≡I where X=O; R³ is attached in the 4-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 2-position; Q=Q²; R²¹=CH₃ and R²²=H), in particular to the compounds I1b1.n, where the variables R¹ to R⁴ and R²⁰ (which in this case corresponds to R⁶) are as defined in Table 1.

Extraordinary preference is also given to the compounds I1b2 (≡I where X=O; R³ is attached in the 4-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 2-position; Q=Q²; R²¹=CH₂CH₃ and R²²=H), in particular to the compounds I1b2.n, where the variables R¹ to R⁴ and R²⁰ (which in this case corresponds to R⁶) are as defined in Table 1.

Extraordinary preference is also given to the compounds I1b3 (≡I where X=O; R³ is attached in the 4-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 2-position; Q=Q²; R²¹=CH(CH₃)₂ and R²²=H), in particular to the compounds I1b3.n, where the variables R¹ to R⁴ and R²⁰ (which in this case corresponds to R⁶) are as defined in Table 1.

Extraordinary preference is also given to the compounds I1b4 (≡I where X=O; R³ is attached in the 4-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 2-position; Q=Q²; R²¹=C(CH₃)₃ and R²²=H), in particular to the compounds I1b4.n, where the variables R¹ to R⁴ and R²⁰ (which in this case corresponds to R⁶) are as defined in Table 1.

Extraordinary preference is also given to the compounds I1b5 (≡I where X=O; R³ is attached in the 4-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 2-position; Q=Q²; R²¹=CH₂CF₃ and R²²=H), in particular to the compounds I1b5.n, where the variables R¹ to R⁴ and R²⁰ (which in this case corresponds to R⁶) are as defined in Table 1.

Extraordinary preference is also given to the compounds I1b6 (≡where X=O; R³ is attached in the 4-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 2-position; Q=Q²; R²¹=CH₃ and R²²=CH₃), in particular to the compounds I1b6.n, where the variables R¹ to R⁴ and R²⁰ (which in this case corresponds to R⁶) are as defined in Table 1.

Extraordinary preference is also given to the compounds I1b7 (≡I where X=O; R³ is attached in the 4-position, R⁴ is attached in the 5-position and “P(═X)R¹R⁷” is attached in the 2-position; Q=Q²; R²¹=CH₂CH₃ and R²²=CH₃), in particular to the compounds I1b7.n, where the variables R¹ to R⁴ and R²⁰ (which in this case corresponds to R⁶) are as defined in Table 1.

Extraordinary preference is also given to the compounds I1b8 (≡I where X=O; R³ is attached in the 4-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 2-position; Q=Q²; R²¹=CH(CH₃)₂ and R²²=CH₃), in particular to the compounds I1b8.n, where the variables R¹ to R⁴ and R²⁰ (which in this case corresponds to R⁶) are as defined in Table 1.

Extraordinary preference is also given to the compounds I1b9 (≡I where X=O; R³ is attached in the 4-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 2-position; Q=Q²; R²¹=C(CH₃)₃ and R²²=CH₃), in particular to the compounds I1b9.n, where the variables R¹ to R⁴ and R²⁰ (which in this case corresponds to R⁶) are as defined in Table 1.

Extraordinary preference is also given to the compounds I1b10 (≡I where X=O; R³ is attached in the 4-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 2-position; Q=Q²; R²¹=CH₂CH₃ and R²²=CH₃), in particular to the compounds I1b10.n, where the variables R¹ to R⁴ and R²⁰ (which in this case corresponds to R⁶) are as defined in Table 1.

Extraordinary preference is also given to the compounds I1b11 (≡I where X=O; R³ is attached in the 4-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 2-position; Q=Q²; R²¹=CH₃ and R²²=CH₃), in particular to the compounds I1b11.n, where the variables R¹ to R⁴ and R²⁰ (which in this case corresponds to R⁶) are as defined in Table 1.

Extraordinary preference is also given to the compounds I1b12 (≡I where X=O; R³ is attached in the 4-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 2-position; Q=Q²; R²¹=CH₂CH₃ and R²²=CF₃), in particular to the compounds I1b12.n, where the variables R¹ to R⁴ and R²⁰ (which in this case corresponds to R⁶) are as defined in Table 1.

Extraordinary preference is also given to the compounds I1b13 (≡I where X=O; R³ is attached in the 4-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 2-position; Q=Q²; R²¹=CH(CH₃)₂ and R²²=CF₃), in particular to the compounds I1b13.n, where the variables R¹ to R⁴ and R²⁰ (which in this case corresponds to R⁶) are as defined in Table 1.

Extraordinary preference is also given to the compounds I1b14 (≡I where X=O; R³ is attached in the 4-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 2-position; Q=Q²; R²¹=C(CH₃)₃ and R²²=CF₃), in particular to the compounds I1b14.n, where the variables R¹ to R⁴ and R²⁰ (which in this case corresponds to R⁶) are as defined in Table 1.

Extraordinary preference is also given to the compounds I1b15 (≡I where X=O; R³ is attached in the 4-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 2-position; Q=Q²; R²¹=CH₂CF₃ and R²²=CF₃), in particular to the compounds I1b15.n, where the variables R¹ to R⁴ and R²⁰ (which in this case corresponds to R⁶) are as defined in Table 1.

Extraordinary preference is also given to the compounds I2b1 (≡I where X=O; R³ is attached in the 2-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 4-position; Q=Q²; R²¹=CH₃ and R²²=H), in particular to the compounds I2b1.n, where the variables R¹ to R⁴ and R²⁰ (which in this case corresponds to R⁶) are as defined in Table 1.

Extraordinary preference is also given to the compounds I2b2 (≡I where X=O; R³ is attached in the 2-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 4-position; Q=Q²; R²¹=CH₂CH₃ and R²²=H), in particular to the compounds I2b2.n, where the variables R¹ to R⁴ and R²⁰ (which in this case corresponds to R⁶) are as defined in Table 1.

Extraordinary preference is also given to the compounds I2b3 (≡I where X=O; R³ is attached in the 2-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 4-position; Q=Q²; R²¹=CH(CH₃)₂ and R²²=H), in particular to the compounds I2b3.n, where the variables R¹ to R⁴ and R²⁰ (which in this case corresponds to R⁶) are as defined in Table 1.

Extraordinary preference is also given to the compounds I2b4 (≡I where X=O; R³ is attached in the 2-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 4-position; Q=Q²; R²¹=C(CH₃)₃ and R²²=H), in particular to the compounds I2b4.n, where the variables R¹ to R⁴ and R²⁰ (which in this case corresponds to R⁶) are as defined in Table 1.

Extraordinary preference is also given to the compounds I2b5 (≡I where X=O; R³ is attached in the 2-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 4-position; Q=Q²; R²¹=CH₂CF₃ and R²²=H), in particular to the compounds I2b5.n, where the variables R¹ to R⁴ and R²⁰ (which in this case corresponds to R⁶) are as defined in Table 1.

Extraordinary preference is also given to the compounds I2b6 (≡I where X=O; R³ is attached in the 2-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 4-position; Q=Q²; R²¹=CH₃ and R²²=CH₃), in particular to the compounds I2b6.n, where the variables R¹ to R⁴ and R²⁰ (which in this case corresponds to R⁶) are as defined in Table 1.

Extraordinary preference is also given to the compounds I2b7 (≡I where X=O; R³ is attached in the 2-position, R⁴ is attached in the 5-position and “P(═X)R¹R⁷” is attached in the 24-position; Q=Q²; R²¹=CH₂CH₃ and R²²=CH₃), in particular to the compounds I2b7.n, where the variables R¹ to R⁴ and R²⁰ (which in this case corresponds to R⁶) are as defined in Table 1.

Extraordinary preference is also given to the compounds I2b8 (≡I where X=O; R³ is attached in the 2-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 4-position; Q=Q²; R²¹=CH(CH₃)₂ and R²²=CH₃), in particular to the compounds I2b8.n, where the variables R¹ to R⁴ and R²⁰ (which in this case corresponds to R⁶) are as defined in Table 1.

Extraordinary preference is also given to the compounds I1b9 (≡I where X=O; R³ is attached in the 2-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 4-position; Q=Q²; R²¹=C(CH₃)₃ and R²²=CH₃), in particular to the compounds I2b9.n, where the variables R¹ to R⁴ and R²⁰ (which in this case corresponds to R⁶) are as defined in Table 1.

Extraordinary preference is also given to the compounds I2b10 (≡I where X=O; R³ is attached in the 2-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 4-position; Q=Q²; R²¹=CH₂CF₃ and R²²=CH₃), in particular to the compounds I2b10.n, where the variables R¹ to R⁴ and R²⁰ (which in this case corresponds to R⁶) are as defined in Table 1.

Extraordinary preference is also given to the compounds I2b11 (≡I where X=O; R³ is attached in the 2-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 4-position; Q=Q²; R²¹=CH₃ and R²²=CF₃), in particular to the compounds I2b11.n, where the variables R¹ to R⁴ and R²⁰ (which in this case corresponds to R⁶) are as defined in Table 1.

Extraordinary preference is also given to the compounds I2b12 (≡I where X=O; R³ is attached in the 2-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 4-position; Q=Q²; R²¹=CH₂CH₃ and R²²=CF₃), in particular to the compounds I2b12.n, where the variables R¹ to R⁴ and R²⁰ (which in this case corresponds to R⁶) are as defined in Table 1.

Extraordinary preference is also given to the compounds I2b13(≡I where X=O; R³ is attached in the 2-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 4-position; Q=Q²; R²¹=CH(CH₃)₂ and R²²=CF₃), in particular to the compounds I2b13.n, where the variables R¹ to R⁴ and R²⁰ (which in this case corresponds to R⁶) are as defined in Table 1.

Extraordinary preference is also given to the compounds I1b14 (≡I where X=O; R³ is attached in the 2-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 4-position; Q=Q²; R²¹=C(CH₃)₃ and R²²=CF₃), in particular to the compounds I2b14.n, where the variables R¹ to R⁴ and R²⁰ (which in this case corresponds to R⁶) are as defined in Table 1.

Extraordinary preference is also given to the compounds I2b15 (≡I where X=O; R³ is attached in the 2-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 4-position; Q=Q²; R²¹=CH₂CF₃ and R²²=CF₃), in particular to the compounds I2b15.n, where the variables R¹ to R⁴ and R²⁰ (which in this case corresponds to R⁶) are as defined in Table 1.

Extraordinary preference is also given to the compounds I1c1 (≡I where X=O; R³ is attached in the 4-position and “P(═X)R¹R²” is attached in the 2-position; Q=Q³; 1=0, R²³=cyclopropyl and R²⁴=H), in particular to the compounds Ic1.n, where the variables R¹ to R³ are as defined in Table 2.

TABLE 2 n R¹ R² R³ 1 H H H 2 CH₃ CH₃ H 3 CH₂CH₃ CH₂CH₃ H 4 CH₂CH₂CH₃ CH₂CH₂CH₃ H 5 OCH₃ OCH₃ H 6 OCH₂CH₃ OCH₂CH₃ H 7 OCH₂CH₂CH₃ OCH₂CH₂CH₃ H 8 SCH₃ SCH₃ H 9 SCH₂CH₃ SCH₂CH₃ H 10 N(CH₃)₂ N(CH₃)₂ H 11 N(CH₂CH₃)₂ N(CH₂CH₃)₂ H 12 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) H 13 O—(CH₂CH₂)—O H 14 O—(CH₂CH₂CH₂)—O H 15 S—(CH₂CH₂)—S H 16 S—(CH₂CH₂CH₂)—S H 17 —(CH₂)₄— H 18 —(CH₂)₅— H 19 H H NO₂ 20 CH₃ CH₃ NO₂ 21 CH₂CH₃ CH₂CH₃ NO₂ 22 CH₂CH₂CH₃ CH₂CH₂CH₃ NO₂ 23 OCH₃ OCH₃ NO₂ 24 OCH₂CH₃ OCH₂CH₃ NO₂ 25 OCH₂CH₂CH₃ OCH₂CH₂CH₃ NO₂ 26 SCH₃ SCH₃ NO₂ 27 SCH₂CH₃ SCH₂CH₃ NO₂ 28 N(CH₃)₂ N(CH₃)₂ NO₂ 29 N(CH₂CH₃)₂ N(CH₂CH₃)₂ NO₂ 30 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) NO₂ 31 O—(CH₂CH₂)—O NO₂ 32 O—(CH₂CH₂CH₂)—O NO₂ 33 S—(CH₂CH₂)—S NO₂ 34 S—(CH₂CH₂CH₂)—S NO₂ 35 —(CH₂)₄— NO₂ 36 —(CH₂)₅— NO₂ 37 H H CN 38 CH₃ CH₃ CN 39 CH₂CH₃ CH₂CH₃ CN 40 CH₂CH₂CH₃ CH₂CH₂CH₃ CN 41 OCH₃ OCH₃ CN 42 OCH₂CH₃ OCH₂CH₃ CN 43 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CN 44 SCH₃ SCH₃ CN 45 SCH₂CH₃ SCH₂CH₃ CN 46 N(CH₃)₂ N(CH₃)₂ CN 47 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CN 48 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CN 49 O—(CH₂CH₂)—O CN 50 O—(CH₂CH₂CH₂)—O CN 51 S—(CH₂CH₂)—S CN 52 S—(CH₂CH₂CH₂)—S CN 53 —(CH₂)₄— CN 54 —(CH₂)₅— CN 55 H H F 56 CH₃ CH₃ F 57 CH₂CH₃ CH₂CH₃ F 58 CH₂CH₂CH₃ CH₂CH₂CH₃ F 59 OCH₃ OCH₃ F 60 OCH₂CH₃ OCH₂CH₃ F 61 OCH₂CH₂CH₃ OCH₂CH₂CH₃ F 62 SCH₃ SCH₃ F 63 SCH₂CH₃ SCH₂CH₃ F 64 N(CH₃)₂ N(CH₃)₂ F 65 N(CH₂CH₃)₂ N(CH₂CH₃)₂ F 66 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) F 67 O—(CH₂CH₂)—O F 68 O—(CH₂CH₂CH₂)—O F 69 S—(CH₂CH₂)—S F 70 S—(CH₂CH₂CH₂)—S F 71 —(CH₂)₄— F 72 —(CH₂)₅— F 73 H H Cl 74 CH₃ CH₃ Cl 75 CH₂CH₃ CH₂CH₃ Cl 76 CH₂CH₂CH₃ CH₂CH₂CH₃ Cl 77 OCH₃ OCH₃ Cl 78 OCH₂CH₃ OCH₂CH₃ Cl 79 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Cl 80 SCH₃ SCH₃ Cl 81 SCH₂CH₃ SCH₂CH₃ Cl 82 N(CH₃)₂ N(CH₃)₂ Cl 83 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Cl 84 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Cl 85 O—(CH₂CH₂)—O Cl 86 O—(CH₂CH₂CH₂)—O Cl 87 S—(CH₂CH₂)—S Cl 88 S—(CH₂CH₂CH₂)—S Cl 89 —(CH₂)₄— Cl 90 —(CH₂)₅— Cl 91 H H Br 92 CH₃ CH₃ Br 93 CH₂CH₃ CH₂CH₃ Br 94 CH₂CH₂CH₃ CH₂CH₂CH₃ Br 95 OCH₃ OCH₃ Br 96 OCH₂CH₃ OCH₂CH₃ Br 97 OCH₂CH₂CH₃ OCH₂CH₂CH₃ Br 98 SCH₃ SCH₃ Br 99 SCH₂CH₃ SCH₂CH₃ Br 100 N(CH₃)₂ N(CH₃)₂ Br 101 N(CH₂CH₃)₂ N(CH₂CH₃)₂ Br 102 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) Br 103 O—(CH₂CH₂)—O Br 104 O—(CH₂CH₂CH₂)—O Br 105 S—(CH₂CH₂)—S Br 106 S—(CH₂CH₂CH₂)—S Br 107 —(CH₂)₄— Br 108 —(CH₂)₅— Br 109 H H CH₃ 110 CH₃ CH₃ CH₃ 111 CH₂CH₃ CH₂CH₃ CH₃ 112 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₃ 113 OCH₃ OCH₃ CH₃ 114 OCH₂CH₃ OCH₂CH₃ CH₃ 115 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₃ 116 SCH₃ SCH₃ CH₃ 117 SCH₂CH₃ SCH₂CH₃ CH₃ 118 N(CH₃)₂ N(CH₃)₂ CH₃ 119 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₃ 120 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₃ 121 O—(CH₂CH₂)—O CH₃ 122 O—(CH₂CH₂CH₂)—O CH₃ 123 S—(CH₂CH₂)—S CH₃ 124 S—(CH₂CH₂CH₂)—S CH₃ 125 —(CH₂)₄— CH₃ 126 —(CH₂)₅— CH₃ 127 H H CH₂CH₃ 128 CH₃ CH₃ CH₂CH₃ 129 CH₂CH₃ CH₂CH₃ CH₂CH₃ 130 CH₂CH₂CH₃ CH₂CH₂CH₃ CH₂CH₃ 131 OCH₃ OCH₃ CH₂CH₃ 132 OCH₂CH₃ OCH₂CH₃ CH₂CH₃ 133 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CH₂CH₃ 134 SCH₃ SCH₃ CH₂CH₃ 135 SCH₂CH₃ SCH₂CH₃ CH₂CH₃ 136 N(CH₃)₂ N(CH₃)₂ CH₂CH₃ 137 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CH₂CH₃ 138 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CH₂CH₃ 139 O—(CH₂CH₂)—O CH₂CH₃ 140 O—(CH₂CH₂CH₂)—O CH₂CH₃ 141 S—(CH₂CH₂)—S CH₂CH₃ 142 S—(CH₂CH₂CH₂)—S CH₂CH₃ 143 —(CH₂)₄— CH₂CH₃ 144 —(CH₂)₅— CH₂CH₃ 145 H H CF₃ 146 CH₃ CH₃ CF₃ 147 CH₂CH₃ CH₂CH₃ CF₃ 148 CH₂CH₂CH₃ CH₂CH₂CH₃ CF₃ 149 OCH₃ OCH₃ CF₃ 150 OCH₂CH₃ OCH₂CH₃ CF₃ 151 OCH₂CH₂CH₃ OCH₂CH₂CH₃ CF₃ 152 SCH₃ SCH₃ CF₃ 153 SCH₂CH₃ SCH₂CH₃ CF₃ 154 N(CH₃)₂ N(CH₃)₂ CF₃ 155 N(CH₂CH₃)₂ N(CH₂CH₃)₂ CF₃ 156 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) CF₃ 157 O—(CH₂CH₂)—O CF₃ 158 O—(CH₂CH₂CH₂)—O CF₃ 159 S—(CH₂CH₂)—S CF₃ 160 S—(CH₂CH₂CH₂)—S CF₃ 161 —(CH₂)₄— CF₃ 162 —(CH₂)₅— CF₃ 163 H H OCH₃ 164 CH₃ CH₃ OCH₃ 165 CH₂CH₃ CH₂CH₃ OCH₃ 166 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₃ 167 OCH₃ OCH₃ OCH₃ 168 OCH₂CH₃ OCH₂CH₃ OCH₃ 169 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₃ 170 SCH₃ SCH₃ OCH₃ 171 SCH₂CH₃ SCH₂CH₃ OCH₃ 172 N(CH₃)₂ N(CH₃)₂ OCH₃ 173 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₃ 174 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₃ 175 O—(CH₂CH₂)—O OCH₃ 176 O—(CH₂CH₂CH₂)—O OCH₃ 177 S—(CH₂CH₂)—S OCH₃ 178 S—(CH₂CH₂CH₂)—S OCH₃ 179 —(CH₂)₄— OCH₃ 180 —(CH₂)₅— OCH₃ 181 H H OCH₂CH₃ 182 CH₃ CH₃ OCH₂CH₃ 183 CH₂CH₃ CH₂CH₃ OCH₂CH₃ 184 CH₂CH₂CH₃ CH₂CH₂CH₃ OCH₂CH₃ 185 OCH₃ OCH₃ OCH₂CH₃ 186 OCH₂CH₃ OCH₂CH₃ OCH₂CH₃ 187 OCH₂CH₂CH₃ OCH₂CH₂CH₃ OCH₂CH₃ 188 SCH₃ SCH₃ OCH₂CH₃ 189 SCH₂CH₃ SCH₂CH₃ OCH₂CH₃ 190 N(CH₃)₂ N(CH₃)₂ OCH₂CH₃ 191 N(CH₂CH₃)₂ N(CH₂CH₃)₂ OCH₂CH₃ 192 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) OCH₂CH₃ 193 O—(CH₂CH₂)—O OCH₂CH₃ 194 O—(CH₂CH₂CH₂)—O OCH₂CH₃ 195 S—(CH₂CH₂)—S OCH₂CH₃ 196 S—(CH₂CH₂CH₂)—S OCH₂CH₃ 197 —(CH₂)₄— OCH₂CH₃ 198 —(CH₂)₅— OCH₂CH₃ 199 H H SCH₃ 200 CH₃ CH₃ SCH₃ 201 CH₂CH₃ CH₂CH₃ SCH₃ 202 CH₂CH₂CH₃ CH₂CH₂CH₃ SCH₃ 203 OCH₃ OCH₃ SCH₃ 204 OCH₂CH₃ OCH₂CH₃ SCH₃ 205 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SCH₃ 206 SCH₃ SCH₃ SCH₃ 207 SCH₂CH₃ SCH₂CH₃ SCH₃ 208 N(CH₃)₂ N(CH₃)₂ SCH₃ 209 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SCH₃ 210 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SCH₃ 211 O—(CH₂CH₂)—O SCH₃ 212 O—(CH₂CH₂CH₂)—O SCH₃ 213 S—(CH₂CH₂)—S SCH₃ 214 S—(CH₂CH₂CH₂)—S SCH₃ 215 —(CH₂)₄— SCH₃ 216 —(CH₂)₅— SCH₃ 217 H H SO₂CH₃ 218 CH₃ CH₃ SO₂CH₃ 219 CH₂CH₃ CH₂CH₃ SO₂CH₃ 220 CH₂CH₂CH₃ CH₂CH₂CH₃ SO₂CH₃ 221 OCH₃ OCH₃ SO₂CH₃ 222 OCH₂CH₃ OCH₂CH₃ SO₂CH₃ 223 OCH₂CH₂CH₃ OCH₂CH₂CH₃ SO₂CH₃ 224 SCH₃ SCH₃ SO₂CH₃ 225 SCH₂CH₃ SCH₂CH₃ SO₂CH₃ 226 N(CH₃)₂ N(CH₃)₂ SO₂CH₃ 227 N(CH₂CH₃)₂ N(CH₂CH₃)₂ SO₂CH₃ 228 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) SO₂CH₃ 229 O—(CH₂CH₂)—O SO₂CH₃ 230 O—(CH₂CH₂CH₂)—O SO₂CH₃ 231 S—(CH₂CH₂)—S SO₂CH₃ 232 S—(CH₂CH₂CH₂)—S SO₂CH₃ 233 —(CH₂)₄— SO₂CH₃ 234 —(CH₂)₅— SO₂CH₃ 235 H H PO(OCH₃)₂ 236 CH₃ CH₃ PO(OCH₃)₂ 237 CH₂CH₃ CH₂CH₃ PO(OCH₃)₂ 238 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₃)₂ 239 OCH₃ OCH₃ PO(OCH₃)₂ 240 OCH₂CH₃ OCH₂CH₃ PO(OCH₃)₂ 241 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₃)₂ 242 SCH₃ SCH₃ PO(OCH₃)₂ 243 SCH₂CH₃ SCH₂CH₃ PO(OCH₃)₂ 244 N(CH₃)₂ N(CH₃)₂ PO(OCH₃)₂ 245 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₃)₂ 246 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₃)₂ 247 O—(CH₂CH₂)—O PO(OCH₃)₂ 248 O—(CH₂CH₂CH₂)—O PO(OCH₃)₂ 249 S—(CH₂CH₂)—S PO(OCH₃)₂ 250 S—(CH₂CH₂CH₂)—S PO(OCH₃)₂ 251 —(CH₂)₄— PO(OCH₃)₂ 252 —(CH₂)₅— PO(OCH₃)₂ 253 H H PO(OCH₂CH₃)₂ 254 CH₃ CH₃ PO(OCH₂CH₃)₂ 255 CH₂CH₃ CH₂CH₃ PO(OCH₂CH₃)₂ 256 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(OCH₂CH₃)₂ 257 OCH₃ OCH₃ PO(OCH₂CH₃)₂ 258 OCH₂CH₃ OCH₂CH₃ PO(OCH₂CH₃)₂ 259 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(OCH₂CH₃)₂ 260 SCH₃ SCH₃ PO(OCH₂CH₃)₂ 261 SCH₂CH₃ SCH₂CH₃ PO(OCH₂CH₃)₂ 262 N(CH₃)₂ N(CH₃)₂ PO(OCH₂CH₃)₂ 263 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(OCH₂CH₃)₂ 264 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(OCH₂CH₃)₂ 265 O—(CH₂CH₂)—O PO(OCH₂CH₃)₂ 266 O—(CH₂CH₂CH₂)—O PO(OCH₂CH₃)₂ 267 S—(CH₂CH₂)—S PO(OCH₂CH₃)₂ 268 S—(CH₂CH₂CH₂)—S PO(OCH₂CH₃)₂ 269 —(CH₂)₄— PO(OCH₂CH₃)₂ 270 —(CH₂)₅— PO(OCH₂CH₃)₂ 271 H H PO(CH₃)₂ 272 CH₃ CH₃ PO(CH₃)₂ 273 CH₂CH₃ CH₂CH₃ PO(CH₃)₂ 274 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₃)₂ 275 OCH₃ OCH₃ PO(CH₃)₂ 276 OCH₂CH₃ OCH₂CH₃ PO(CH₃)₂ 277 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₃)₂ 278 SCH₃ SCH₃ PO(CH₃)₂ 279 SCH₂CH₃ SCH₂CH₃ PO(CH₃)₂ 280 N(CH₃)₂ N(CH₃)₂ PO(CH₃)₂ 281 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₃)₂ 282 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₃)₂ 283 O—(CH₂CH₂)—O PO(CH₃)₂ 284 O—(CH₂CH₂CH₂)—O PO(CH₃)₂ 285 S—(CH₂CH₂)—S PO(CH₃)₂ 286 S—(CH₂CH₂CH₂)—S PO(CH₃)₂ 287 —(CH₂)₄— PO(CH₃)₂ 288 —(CH₂)₅— PO(CH₃)₂ 289 H H PO(CH₂CH₃)₂ 290 CH₃ CH₃ PO(CH₂CH₃)₂ 291 CH₂CH₃ CH₂CH₃ PO(CH₂CH₃)₂ 292 CH₂CH₂CH₃ CH₂CH₂CH₃ PO(CH₂CH₃)₂ 293 OCH₃ OCH₃ PO(CH₂CH₃)₂ 294 OCH₂CH₃ OCH₂CH₃ PO(CH₂CH₃)₂ 295 OCH₂CH₂CH₃ OCH₂CH₂CH₃ PO(CH₂CH₃)₂ 296 SCH₃ SCH₃ PO(CH₂CH₃)₂ 297 SCH₂CH₃ SCH₂CH₃ PO(CH₂CH₃)₂ 298 N(CH₃)₂ N(CH₃)₂ PO(CH₂CH₃)₂ 299 N(CH₂CH₃)₂ N(CH₂CH₃)₂ PO(CH₂CH₃)₂ 300 N(CH₃)(CH₂CH₃) N(CH₃)(CH₂CH₃) PO(CH₂CH₃)₂ 301 O—(CH₂CH₂)—O PO(CH₂CH₃)₂ 302 O—(CH₂CH₂CH₂)—O PO(CH₂CH₃)₂ 303 S—(CH₂CH₂)—S PO(CH₂CH₃)₂ 304 S—(CH₂CH₂CH₂)—S PO(CH₂CH₃)₂ 305 —(CH₂)₄— PO(CH₂CH₃)₂ 306 —(CH₂)₅— PO(CH₂CH₃)₂

Extraordinary preference is also given to the compounds I1c2 (≡I where X=O; R³ is attached in the 4-position, R⁴ in the 5-position and “P(═X)R¹R²” in the 2-position; Q=Q³; R⁴=CH₃, R²³=cyclopropyl and R²⁴=H), in particular to the compounds I1c2.n, where the variables R¹ to R³ are as defined in Table 2.

Extraordinary preference is also given to the compounds I1c3 (≡I where X=O; R³ is attached in the 4-position, R⁴ in the 5-position and “P(═X)R¹R²” in the 2-position; Q=Q³; R⁴=Cl, R²³=cyclopropyl and R²⁴=H), in particular to the compounds I1c3.n, where the variables R¹ to R³ are as defined in Table 2.

Extraordinary preference is also given to the compounds I1c4 (≡I where X=O; R³ is attached in the 4-position, R⁴ in the 5-position and “P(═X)R¹R²” in the 2-position; Q=Q³; R⁴=Br, R²³=cyclopropyl and R²⁴=H), in particular to the compounds I1c4, where the variables R¹ to R³ are as defined in Table 2.

Extraordinary preference is also given to the compounds I2cl (≡I where X=O; R³ is attached in the 2-position and “P(═X)R¹R²” is attached in the 4-position; Q=Q³; 1=0; R²³=cyclopropyl and R²⁴=H), in particular to the compounds I2c1.n, where the variables R¹ to R³ are as defined in Table 2.

Extraordinary preference is also given to the compounds I2c2 (≡I where X=O; R³ is attached in the 2-position, R⁴ in the 5-position and “P(═X)R¹R²” in the 4-position; Q=Q³; R⁴=CH₃, R²³=cyclopropyl and R²⁴=H), in particular to the compounds I2c2.n, where the variables R¹ to R³ are as defined in Table 2.

Extraordinary preference is also given to the compounds I2c3 (≡I where X=O; R³ is attached in the 2-position, R⁴ in the 5-position and “P(═X)R¹R²” in the 2-position; Q=Q³; R⁴=Cl, R²³=cyclopropyl and R²⁴=H), in particular to the compounds I2c3.n, where the variables R¹ to R³ are as defined in Table 2.

Extraordinary preference is also given to the compounds I2c4 (≡I where X=O; R³ is attached in the 2-position, R⁴ in the 5-position and “P(═X)R¹R²” in the 4-position; Q=Q³; R⁴=Br, R²³=cyclopropyl and R²⁴=H), in particular to the compounds I2c4, where the variables R¹ to R³ are as defined in Table 2.

Extraordinary preference is also given to the compounds I1d1 (≡I where X=O; R³ is attached in the 4-position and “P(═X)R¹R²” is attached in the 2-position; Q=Q⁴; 1=0; R²⁵=cyclopropyl), in particular to the compounds I1d1.n, where the variables R¹ to R³ are as defined in Table 2.

Extraordinary preference is also given to the compounds I1d2 (≡I where X=O; R³ is attached in the 4-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 2-position; Q=Q⁴; R⁴=CH₃, R²⁵=cyclopropyl), in particular to the compounds I1d2.n, where the variables R¹ to R³ are as defined in Table 2.

Extraordinary preference is also given to the compounds I1d3 (≡I where X=O; R³ is attached in the 4-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 2-position; Q=Q⁴; R⁴=Cl, R²⁵=cyclopropyl), in particular to the compounds I1d3.n, where the variables R¹ to R³ are as defined in Table 2.

Extraordinary preference is also given to the compounds I1d4 (≡I where X=O; R³ is attached in the 4-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 2-position; Q=Q⁴; R⁴=Br, R²⁵=cyclopropyl), in particular to the compounds I1d4, where the variables R¹ to R³ are as defined in Table 2.

Extraordinary preference is also given to the compounds I2d1 (≡I where X=O; R³ is attached in the 2-position and “P(═X)R¹R²” is attached in the 4-position; Q=Q⁴; 1=0; R²⁵=cyclopropyl), in particular to the compounds I2d1.n, where the variables R¹ to R³ are as defined in Table 2.

Extraordinary preference is also given to the compounds I2d2 (≡I where X=O; R³ is attached in the 4-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 2-position; Q=Q⁴; R⁴=CH₃, R²⁵=cyclopropyl), in particular to the compounds I2a2.n, where the variables R¹ to R³ are as defined in Table 2.

Extraordinary preference is also given to the compounds I2d3 (≡I where X=O; R³ is attached in the 2-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 2-position; Q=Q⁴; R⁴=Cl, R²⁵=cyclopropyl), in particular to the compounds I2d3.n, where the variables R¹ to R³ are as defined in Table 2.

Extraordinary preference is also given to the compounds I2d4 (≡I where X=O; R³ is attached in the 4-position, R⁴ is attached in the 5-position and “P(═X)R¹R²” is attached in the 2-position; Q=Q⁴; R⁴=Br, R²⁵=cyclopropyl), in particular to the compounds I2d4, where the variables R¹ to R³ are as defined in Table 2.

The phosphorus-containing benzoyl derivatives of the formula I can be obtained by different routes, for example by the following processes:

A. Preparation of compounds of the formula Ia where R⁶=halogen by reaction of compounds of the formula Ia (≡I where Q=Q¹) where R⁶=hydroxyl with halogenating agents:

Suitable halogenating agents are, for example, phosgene, diphosgene, triphosgene, thionyl chloride, oxalyl chloride, phosphorus oxychloride, phosphorus pentachloride, mesyl chloride, chloromethylene-N,N-dimethylammonium chloride, oxalyl bromide, phosphorus oxybromide, etc.

The starting materials are generally employed in equimolar amounts. However, it may also be advantageous to employ an excess of one or the other component.

Suitable solvents are, for example, chlorinated hydrocarbons, such as methylene chloride or 1,2-dichloroethane, aromatic hydrocarbons, for example toluene, xylene or chlorobenzene, polar aprotic solvents, such as acetonitrile, dimethylformamide or dimethyl sulfoxide, or mixtures of these. However, it is also possible to carry out the reaction without a solvent.

In general, the reaction temperature is in the range from 0° C. to the boiling point of the reaction mixture.

Work-up can be carried out in a manner known per se to afford the product.

B. Preparation of compounds of the formula Ia (≡I where Q=Q¹) where R⁶=OR¹³, OSO₂R¹⁴, OPR¹⁵R¹⁶, OPOR¹⁵R¹⁶ or OPSR¹⁵R¹⁶ by reaction of compounds of the formula Ia (≡I where Q=Q¹) where R⁶=hydroxyl with alkylating, sulfonylating or phosphonylating agents IIα, IIβ, IIγ, IIδ or IIε.

L¹ is a nucleophilically replaceable leaving group, such as halogen, for example chlorine or bromine, hetaryl, for example imidazolyl, carboxylate, for example acetate, or sulfonate, for example mesylate or triflate, etc.

The compounds of the formula IIα, IIβ, IIγ, IIδ or IIε can be employed directly, such as in the case of the carbonyl halides, or generated in situ, for example activated carboxylic acids (using carboxylic acid and dicyclohexylcarbodiimide, etc.).

The starting materials are generally employed in equimolar amounts. However, it may also be advantageous to employ an excess of one or the other component.

If appropriate, it may also be advantageous to carry out the reaction in the presence of a base. The reactants and the base are advantageously employed in equimolar amounts. In certain cases, an excess of base of, for example, 1.5 to 3 molar equivalents may be advantageous.

Suitable bases are tertiary alkylamines, such as triethylamine, aromatic amines, such as pyridine, alkali metal carbonates, for example sodium carbonate or potassium carbonate, alkali metal bicarbonates, such as sodium bicarbonate and potassium bicarbonate, alkali metal alkoxides, such as sodium methoxide, sodium ethoxide, potassium tert-butoxide, or alkali metal hydrides, for example sodium hydride. Preference is given to using triethylamine or pyridine.

Suitable solvents are, for example, chlorinated hydrocarbons, such as methylene chloride or 1,2-dichloroethane, aromatic hydrocarbons, for example toluene, xylene or chlorobenzene, ethers, such as diethyl ether, methyl tert-butyl ether, tetrahydrofuran or dioxane, polar aprotic solvents, such as acetonitrile, dimethylformamide or dimethyl sulfoxide, or esters, such as ethyl acetate, or mixtures of these.

The reaction temperature is generally in the range from 0° C. to the boiling point of the reaction mixture.

Work-up can be carried out in a manner known per se to afford the product.

C. Preparation of compounds of the formula Ia (≡I where Q=Q¹) where R⁶=OR¹³, SR¹³, POR¹⁵R¹⁶, NR¹⁷R¹⁸, ONR¹⁸R¹⁹, N-bonded heterocyclyl or O-(N-bonded heterocyclyl) by reaction of compounds of the formula Ia (≡I where Q=Q¹) where R⁶=halogen, OSO₂R¹⁴ with compounds of the formula IIIα, IIIβ, IIIγ, IIIδ, IIIε, IIIη or IIIΘ, if appropriate in the presence of a base or with prior salt formation.

The starting materials are employed in equimolar amounts. However, it may also be advantageous to employ an excess of one or the other component.

If appropriate, it may also be advantageous to carry out the reaction in the presence of a base. The reactants and the base are advantageously employed in equimolar amounts. An excess of base of, for example, from 1.5 to 3 molar equivalents, based on Ia (≡I where Q=Q¹) where R⁶=halogen, OSO₂R¹⁴, may be advantageous in certain cases.

Suitable bases are tertiary alkylamines, such as triethylamine, aromatic amines, such as pyridine, alkali metal carbonates, for example sodium carbonate or potassium carbonate, alkali metal bicarbonates, such as sodium bicarbonate and potassium bicarbonate, alkali metal alkoxides, such as sodium methoxide, sodium ethoxide, potassium tert-butoxide, or alkali metal hydrides, for example sodium hydride. Preference is given to using sodium hydride or potassium tert-butoxide.

Suitable solvents are, for example, chlorinated hydrocarbons, such as methylene chloride or 1,2-dichloroethane, aromatic hydrocarbons, for example toluene, xylene or chlorobenzene, ethers, such as diethyl ether, methyl tert-butyl ether, tetrahydrofuran or dioxane, polar aprotic solvents, such as acetonitrile, dimethylformamide or dimethyl sulfoxide, or mixtures of these.

In general, the reaction temperature is in the range from 0° C. to the boiling point of the reaction mixture.

Work-up can be carried out in a manner known per se to afford the product.

D. Preparation of compounds of the formula Ia (≡I where Q=Q¹) where R⁶=SOR¹⁴, SO₂R¹⁴ by reaction of compounds of the formula Ia (≡I where Q=Q¹) where R⁶=SR¹⁴ with an oxidizing agent.

Suitable oxidizing agents are, for example, m-chloroperbenzoic acid, peroxyacetic acid, trifluoroperoxyacetic acid, hydrogen peroxide, if appropriate in the presence of a catalyst, such as tungstate.

The starting materials are generally employed in equimolar amounts. However, it may also be advantageous to employ an excess of one or the other component.

Suitable solvents are, for example, chlorinated hydrocarbons, such as methylene chloride or 1,2-dichloroethane, aromatic hydrocarbons, for example toluene, xylene or chlorobenzene, ethers, such as diethyl ether, methyl tert-butyl ether, tetrahydrofuran or dioxane, polar aprotic solvents, such as acetonitrile or dimethylformamide, or esters, such as ethyl acetate, or mixtures of these.

In general, the reaction temperature is in the range from 0° C. to the boiling point of the reaction mixture.

Work-up can be carried out in a manner known per se to afford the product.

E. Preparation of compounds of the formula Ia (≡I where Q=Q¹) where R⁶=OH by reaction of an activated phosphorus-containing benzoic acid of the formula IVα or a phosphorus-containing benzoic acid IVβ, which is preferably activated in situ, with a cyclohexanedione of the formula V to give the acylation product, followed by rearrangement.

L² is a nucleophilically replaceable leaving group, such as halogen, for example bromine or chlorine, hetaryl, for example imidazolyl or pyridyl, carboxylate, for example acetate or trifluoroacetate, etc.

The activated benzoic acid IV can be employed directly, such as in the case of the benzoyl halides, or generated in situ, for example using dicyclohexylcarbodiimide, triphenylphosphine/azodicarboxylic acid ester, 2-pyridine disulfide/triphenylphosphine, carbonyldiimidazole, etc.

If appropriate, it may be advantageous to carry out the acylation reaction in the presence of a base. The reactants and the auxiliary base are advantageously employed in equimolar amounts. A slight excess of auxiliary base, for example from 1. to 1.5 molar equivalents, based on IVα or IVβ, may be advantageous in certain cases.

Suitable auxiliary bases are tertiary alkylamines, pyridine or alkali metal carbonates. Suitable solvents are, for example, chlorinated hydrocarbons, such as methylene chloride or 1,2-dichloroethane, aromatic hydrocarbons, such as toluene, xylene or chlorobenzene, ethers, such as diethyl ether, methyl tert-butyl ether, tetrahydrofuran or dioxane, polar aprotic solvents, such as acetonitrile, dimethylformamide or dimethyl sulfoxide, or esters, such as ethyl acetate, or mixtures of these.

If the activated carboxylic acid component used is a phosphorus-containing benzoyl halide, it may be advantageous to cool the reaction mixture to 0-10° C. when adding this reaction partner. The mixture is subsequently stirred at 20-100° C., preferably at 25-50° C., until the reaction has gone to completion. Work-up is carried out in a customary manner, for example by pouring the reaction mixture into water and extracting the product of value. Solvents which are suitable for this purpose are, in particular, methylene chloride, diethyl ether and ethyl acetate. The organic phase is dried and the solvent is removed, and the crude ester can then be employed for the rearrangement without further purification.

The rearrangement of the esters VI to the compounds of the formula Ia is advantageously carried out at 20-100° C. in a solvent and in the presence of a base and, if appropriate, using a cyano compound as catalyst.

Suitable solvents are, for example, acetonitrile, methylene chloride, 1,2-dichloroethane, dioxane, ethyl acetate, toluene or mixtures of these. Preferred solvents are acetonitrile and dioxane.

Suitable bases are tertiary amines, such as triethylamine, aromatic amines, such as pyridine, or alkali metal carbonates, such as sodium carbonate or potassium carbonate, which are preferably employed in equimolar amounts or in up to four-fold excess, based on the ester. Preference is given to using triethylamine or alkali metal carbonate, preferably in twice the equimolar amount, based on the ester.

Suitable cyano compounds are inorganic cyanides, such as sodium cyanide or potassium cyanide, and organic cyano compounds, such as acetone cyanohydrin or trimethylsilyl cyanide. They are employed in an amount of from 1 to 50 mol percent, based on the ester. Preference is given to using acetone cyanohydrin or trimethylsilyl cyanide, for example in an amount of from 5 to 15, preferably 10, mol percent, based on the ester.

Work-up can be carried out in a manner known per se. The reaction mixture is, for example, acidified with dilute mineral acid, such as 5% strength hydrochloric acid or sulfuric acid, and extracted with an organic solvent, for example methylene chloride or ethyl acetate. The organic extract can be extracted with 5-10% strength alkali metal carbonate solution, for example sodium carbonate or potassium carbonate solution. The aqueous phase is acidified and the resulting precipitate is filtered off with suction and/or the mixture is extracted with methylene chloride or ethyl acetate and the extract is dried and concentrated.

F. Preparation of compounds of the formula Ib (≡I where Q=Q²) where R²⁰=halogen by reaction of compounds of the formula Ib (≡I where Q=Q²) where R²⁰=hydroxyl with halogenating agents:

What has been said in section A applies analogously.

G. Preparation of compounds of the formula Ib (≡I where Q=Q²) where R²⁰=OR¹³, OSO₂R¹⁴, OPR¹⁵R¹⁶, OPOR¹⁵R¹⁶ or OPSR¹⁵R¹⁶ by reaction of compounds of the formula Ib (≡I where Q=Q²) where R⁶=hydroxyl with alkylating, sulfonylating or phosphonylating agents IIα, IIβ, IIγ, IIδ or IIε.

What has been said in section B applies analogously.

H. Preparation of compounds of the formula Ib (≡I where Q=Q²) where R⁶=OR¹³, SR¹³, POR¹⁵R¹⁶, NR¹⁷R¹⁸, ONR¹⁸R¹⁹, N-bonded heterocyclyl or O—(N-bonded heterocyclyl) by reaction of compounds of the formula Ib (≡I where Q=Q²) where R²⁰=halogen, OSO₂R¹⁴ with compounds of the formula IIIα, IIIβ, IIIγ, IIIδ, IIIε, IIIη or IIIΘ, if appropriate in the presence of a base or with prior salt formation.

What has been said in section C applies analogously.

I. Preparation of compounds of the formula Ib (≡I where Q=Q²) where R²⁰=SOR¹⁴, SO₂R¹⁴ by reaction of compounds of the formula Ib (≡I where Q=Q²) where R²⁰=SR¹⁴ with an oxidizing agent.

What has been said in section D applies analogously.

K. Preparation of compounds of the formula Ib (≡I where Q=Q²) where R²⁰≠hydroxyl by reaction of a metallated pyrazole derivative of the formula VII with a phosphorus-containing benzoic acid derivative of the formula VIγ:

M is a metal, in particular an alkali metal, such as lithium or sodium, an alkaline earth metal, such as magnesium, or a transition metal, such as palladium, nickel, etc., and L³ is a nucleophilically replaceable leaving group, such as halogen, for example chlorine or bromine, alkylsulfonate, such as mesylate, haloalkylsulfonate, such as triflate, or cyanide.

The reaction is generally carried out at temperatures from −100° C. to the reflux temperature of the reaction mixture. Suitable solvents are inert aprotic solvents, such as ethers, such as diethyl ether, tetrahydrofuran. The compounds of the formula Ivγ are generally employed in excess; however, it may also be advantageous to employ them in equimolar amounts or substoichiometric amounts. Work-up is carried out to afford the product.

The metallated pyrazole derivatives of the formula VII can be generated in a manner known per se by reacting pyrazoles halogenated in the 4-position with metals such as lithium, sodium, magnesium etc., or with organometallic compounds, for example butyllithium. However, it is also possible to metallate pyrazoles which are linked to hydrogen in the 4-position directly, for example using the abovementioned metals or organometallic compounds. The reactions are generally carried out in an inert aprotic solvent, preferably in ether, such as diethyl ether, tetrahydrofuran, etc. The reaction temperature is in the range from −100° C. to the boiling point of the reaction mixture. The compounds of the formula VII are generally directly reacted further or generated in situ.

L. Preparation of compounds of the formula Ib (≡I where Q=Q²) where R²⁰=hydroxyl by reaction of an activated phosphorus-containing benzoic acid of the formula IVα or a phosphorus-containing benzoic acid IVβ, which is preferably activated in situ, with a pyrazole of the formula VIII to give the acylating product, followed by rearrangement.

What has been said in section E applies analogously.

However, it is also possible to generate the ester IX in situ by reacting a pyrazole of the formula VIII, or an alkali metal salt thereof, with a phosphorus-containing benzene derivative of the formula X in the presence of carbon monoxide, a catalyst and a base.

L⁴ is a leaving group, such as halogen, for example chlorine, bromine or iodine, or sulfonate, such as mesylate or triflate; preference is given to bromine or triflate.

If appropriate, the ester IX reacts directly to give the phosphorus-containing benzoyl derivative of the formula Ib.

Suitable catalysts are palladium-ligand complexes in which the palladium is present in oxidation state 0, metallic palladium, which has optionally been absorbed on a carrier, and preferably palladium(II) salts. The reaction with palladium(II) salts and metallic palladium is preferably carried out in the presence of complex ligands.

An example of a suitable palladium(0)-ligand complex is tetrakis(triphenylphosphine)palladium.

Metallic palladium is preferably absorbed on an inert carrier such as, for example, active carbon, silica, alumina, barium sulfate or calcium carbonate. The reaction is preferably carried out in the presence of complex ligands such as, for example, triphenylphosphine.

Examples of suitable palladium(II) salts are palladium acetate and palladium chloride. The presence of complex ligands such as, for example, triphenylphosphine is preferred.

Suitable complex ligands for the palladium-ligand complexes, or in whose presence the reaction is preferably carried out with metallic palladium or palladium(II) salts, are tertiary phosphines whose structure is represented by the following formulae:

where z is from 1 to 4 and the radicals R^(a) to R^(g) are C₁-C₆-alkyl, aryl-C₁-C₂-alkyl or preferably aryl. Aryl is, for example, naphthyl and unsubstituted or substituted phenyl, such as, for example, 2-tolyl and, in particular, unsubstituted phenyl.

The complex palladium salts can be prepared in a manner known per se starting from commercially obtainable palladium salts such as palladium chloride or palladium acetate and the appropriate phosphines, such as, for example, triphenylphosphine or 1,2-bis(diphenylphosphino)ethane. Many of the complex palladium salts are commercially available. Preferred palladium salts are [(R)(+)-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl]palladium(II) chloride, bis(triphenylphosphine)palladium(II) acetate and, in particular, bis(triphenylphosphine)palladium(II) chloride.

The palladium catalyst is generally employed in a concentration of from 0.05 to 5 mol %, and preferably 1-3 mol %.

Suitable bases are tertiary amines, such as, for example, N-methylpiperidine, ethyldiisopropylamine, 1,8-bisdimethylaminonaphthalene or, in particular, triethylamine. Also suitable are alkali metal carbonates, such as sodium carbonate or potassium carbonate. However, mixtures of potassium carbonate and triethylamine are also suitable.

In general, from 2 to 4 molar equivalents, in particular 2 molar equivalents, of the alkali metal carbonate and from 1 to 4 molar equivalents, in particular 2 molar equivalents, of the tertiary amine are employed, based on the phosphorus-containing benzene derivative of the formula X.

Suitable solvents are nitrites, such as benzonitrile and acetonitrile, amides, such as dimethylformamide, dimethylacetamide, tetra-C₁-C₄-alkylureas or N-methylpyrrolidone and, preferably, ethers such as tetrahydrofuran, methyl tert-butyl ether. Particularly preferred solvents are ethers such as 1,4-dioxane and dimethoxyethane.

M. Preparation of compounds of the formula Ic (≡I where Q=Q³) where R²⁴=H by reaction of a 1,3-dicarbonyl compound of the formula XI with hydroxylamine.

L⁵ is an O—C₁-C₆-alkyl or N(C₁-C₆-alkyl)₂ group. The 1,3-dicarbonyl compound of the formula XI is reacted with hydroxylamine which is generated in situ, for example from hydroxylamine salt using a base or an acid acceptor, such as triethylamine or sodium acetate.

The starting material of the formula XI is obtained by reacting the β-keto esters of the formula XII, which are known per se, with an activated phosphorus-containing benzoic acid IVα. The acylation product XIII is subsequently converted into the 1,3-diketone XIV using, for example, p-toluenesulfonic acid as catalyst in an inert solvent, such as toluene. The 1,3-diketone XIV is subsequently reacted with an orthoester or dimethylformamide dialkyl acetal to give the 1,3-dicarbonyl compound of the formula XI.

N. Preparation of compounds of the formula Ic (≡I where Q=Q³) by cycloaddition of the α,β-unsaturated benzoyl derivative XV with a nitrile oxide of the formula XVI

The α,β-unsaturated benzoyl derivative XV is obtained by ethynylation of the activated phosphorus-containing benzoic acid of the formula IVα.

Z is a metal such as lithium, an organotin radical such as Sn(C₄H₉)₃ or a zinc radical such as ZnCl or ZnBr.

O. Preparation of compounds of the formula Id (≡I where Q=Q⁴) by reaction of the cyanoketone XVII with an activated phosphorus-containing benzoic acid of the formula IVα in the presence of a base such as triethylamine, sodium carbonate, sodium hydride or magnesium ethoxide in an inert organic solvent such as diethyl ether, tetrahydrofuran, N,N-diethylformamide, dichloromethane or acetonitrile.

The phosphorus-containing benzoyl halides of the formula IVα where L²=halogen can be prepared in a manner known per se by reacting the benzoic acids of the formula IVβ with halogenating agents such as thionyl chloride, thionyl bromide, phosgene, diphosgene, triphosgene, oxalyl chloride, oxalyl bromide.

The phosphorus-containing benzoic acids of the formula IVβ can be prepared in a manner known per se by acidic or basic hydrolysis from the corresponding phosphorus-containing benzoic esters IVδ (cf. J. March, “Advanced Organic Chemistry”, 4^(th) edition, Wiley, New York, p. 378 ff.)

where T is C₁-C₆-alkoxy.

The phosphorus-containing benzoic esters IVδ are obtainable by different routes:

They can be obtained by electrophilic or nucleophilic aromatic substitution of benzoic esters of the formula XVIII and, if appropriate, further functionalization of the group thus introduced.

For example, the ester of the formula XVIII can be nitrated analogously to known methods (R³=NO₂; cf. J. March, “Advanced Organic Chemistry”, 4^(th) edition, p. 522 ff.), brominated or chlorinated (R³=Cl, Br; cf. J. March, “Advanced Organic Chemistry”, 4^(th) edition, p. 531 ff.).

The abovementioned electrophilic aromatic substitution reaction may result in mixtures of isomers, which can be separated or purified by distillation, crystallization or chromatographic methods.

Phosphorus-containing benzoic esters of the formula IVδ where R³=NH₂ can be obtained by reduction of the corresponding nitro compounds of the formula IVδ where R³=NO₂.

Suitable reducing agents are, inter alia, metals such as iron or zinc in the presence of hydrochloric acid and catalytically activated hydrogen (cf. J. March, “Advanced Organic Chemistry”, 4^(th) edition, p. 1216 ff.)

Phosphorus-containing benzoic esters of the formula IVδ where R³=(C₁-C₆-alkylsulfonyl)amino, (C₁-C₆-haloalkylsulfonyl)amino can be obtained by reaction of the corresponding amino compounds with appropriately substituted sulfonyl chlorides in the presence of a base (cf.

T. W. Green et al., “Protective Groups in Organic Synthesis”, p. 379 f.)

The latter can be converted into the corresponding N-alkyl derivatives by alkylation in the presence of a base.

Suitable bases are, inter alia, sodium hydride, potassium hydride, potassium tert-butoxide, and suitable alkyl halides are alkyl bromides and alkyl iodides (cf. J. P. Dunn et al., J. Med. Chem. 1981, 24, p. 1097).

Phosphorus-containing benzoic esters of the formula IVδ where R³=halogen, cyano, C₁-C₆-alkyl, C₁-C₆-alkylthio or C₁-C₆-haloalkylthio can be obtained from the corresponding amino compounds by Sandmeyer reaction or related reactions (cf. J. March, “Advanced Organic Chemistry”, 4^(th) edition, pp. 723-724, pp. 669-671)

If appropriate, it may be advantageous to carry out the reactions in the presence of metal catalysts such as, for example, copper(I) or palladium(II) (cf., for example, Kikukawa et al., J. Org. Chem. 1983, 48, 1333).

Phosphorus-containing benzoic esters of the formula IVδ where R³=S(O)_(1,2)—C₁-C₆-alkyl or S(O)_(1,2)—C₁-C₆-haloalkyl can be obtained by reaction of the corresponding sulfur compounds with an oxidizing agent such as bromine, peroxyacetic acid, m-chloroperbenzoic acid and hydrogen peroxide, if appropriate in the presence of a catalyst such as tungstate.

Phosphorus-containing benzoic esters of the formula IVδ here R³=aminosulfonyl, C₁-C₆-alkylaminosulfonyl or di(C₁-C₆-alkyl)aminosulfonyl can be obtained by reaction of the corresponding sulfonyl chloride with ammonia or suitable amines. If appropriate, it may be useful to operate in the presence of a base such as triethylamine, sodium carbonate, potassium carbonate, sodium bicarbonate, potassium bicarbonate or pyridine (cf. J. March, “Advanced Organic Chemistry”, 4^(th) edition, p. 499). The sulfonyl chloride is obtained by sulfochlorination of the corresponding diazonium salt.

Phosphorus-containing benzoic esters of the formula IVδ where R³=C₁-C₆-alkoxy or C₁-C₆-haloalkoxy can be obtained by alkylation of the corresponding phenols in the presence of a base. Suitable bases are, in addition to the customary bases, in particular sodium carbonate, potassium carbonate, sodium hydride or potassium tert-butoxide. Preferred alkylating agents are appropriate halogenated or non-halogenated alkyl bromides or chlorides (cf., for example, H. Fener et al., “The Chemistry of the Ether Linkage”, Wiley, New York, 1967, pp. 445-498.)

The phenols can be obtained by boiling down of corresponding diazonium compounds.

Phosphorus-containing benzoic esters of the formula IVδ where R³=PXR¹R² can be obtained by reaction of compounds of the formula IVδ where R³=Br, I, OSO₂CF₃ etc., with suitable phosphonous acids or phosphorous acids in the presence of a transition metal catalyst such as nickel or palladium and, if appropriate, of a base (cf., for example, T. Hirao et al., Synthesis 1981, 56).

Phosphorus-containing benzoic esters of the formula IVδ where R³=phenyl can be prepared by reaction of a corresponding bromide or iodide of the formula IVδ where R³=Br or I with a phenyl bromide or phenyl iodide, which may be substituted, in the presence of copper (cf. Ranta et al., Synthesis 1974, 9; Goshaer et al., Russ. Chem. Rev. 1972, 41, 1046)

Phosphorus-containing benzoic esters of the formula IVδ where R³=unsub. or sub. phenyl, unsub. or sub. heterocyclyl can be obtained by reaction of compounds of the formula IVδ where R³=a leaving group such as bromine, iodine, triflate, fluorosulfonyloxy, etc., with an unsub. or sub. phenyl or heterocyclyl stannane (Stille coupling), an unsub. or sub. phenyl or heterocyclyl boron compound (Suzuki coupling) or an unsub. or sub. phenyl or heterocyclyl zinc compound (Negishi coupling) in a manner known per se (cf. Tetrahedron Lett. 1986, 27, 5265) in the presence of a palladium or nickel catalyst and, if appropriate, a base.

Ar′=unsub. or sub. phenyl or heterocyclyl

Met=Sn(C₁-C₄-alkyl)₃, B(OH)₂, ZnBr, ZnCl

Phosphorus-containing benzoic esters of the formula IVδ where R³=unsub. or sub. heterocyclyl can also be obtained by constructing the heterocycle from suitable precursors.

1,2,4-Oxadiazoline derivatives, for example, can be prepared from aldoximes of the formula XIX by condensation with aldehydes of the ketones (cf., for example, Arch. Pharm. 1993, 326, 383-389).

The thioamides of the formula XX are suitable precursors for 2-thiazolinyl derivatives (cf., for example, Tetrahedron 1986, 42, 1449-1460) and for 2-thiazolyl derivatives (cf., for example, Houben-Weyl, “Methoden der organischen Chemie”[Methods of Organic Chemistry], 4^(th) edition, Vol. E5, p. 1268 ff. (1985)).

2-Oxazolinyl, 2-thiazolinyl and 2-imidazolinyl derivatives are obtainable from the carboxylic acids of the formula XXI (cf., for example, Tetrahedron Lett. 1981, 22, 4471-4474).

According to processes known from the literature, it is possible to prepare 1,3-thiazole-5(4H)-thion-2-yl or 5-oxo-2-imidazolin-2-yl derivatives from carbonyl halides of the formula XXII where Hal is halogen, in particular from carbonyl chlorides (cf., for example, Helv. Chim. Acta, 1986, 69, 374-388; Heterocycles 1989, 29, 1185-1189).

Furthermore, it is possible to prepare 2-oxazolyl derivatives from the carboxylic acids of the formula XXI or the carbonyl halides of the formula XXII (cf., for example, Heterocyclic Chem. 1991, 28, 17-28).

The conversion of oximes of the formula XXIV into 4,5-dihydroisoxazol-3-yl or isoxazol-3-yl derivatives can be carried out in a manner known per se via the intermediate of the hydroxamoyl chlorides or bromides. Using the latter, nitrile oxides are generated in situ which react with alkenes or alkynes to give the desired products (cf., for example, Chem. Ber. 1973, 106, 3258-3274). 1,3-Dipolar cycloaddition with chlorosulfonyl isocyanate to the nitrile oxide formed in situ affords 1,2,4-oxadiazolin-5-on-3-yl derivatives (cf., for example, Heterocycles 1988, 27, 683-685).

The aldehydes of the formula XXV can be converted into 2,4-dihydro-1,2,4-triazol-3-on-5-yl derivatives via the intermediate of the semicarbazones (cf., for example, J. Heterocyclic Chem. 1986, 23, 881-883).

2-Imidazolinyl derivatives are preparable from benzonitriles of the formula XXVI by known methods (cf., for example, J. Org. Chem. 1987, 52, 1017-1021).

It is also possible to prepare 1,2,4-triazol-3-yl derivatives by known processes from the benzonitriles of the formula XXVI (cf., for example, J. Chem. Soc. 1954, 3461-3464).

The aldehydes XXV can be reacted in a manner known per se by Wittig reaction with phosphonium salts (Ph)₃P⁺CH₂COR*X⁻ (J. March, “Advanced Organic Chemistry”, 3^(rd) edition, p. 864 ff., Wiley-Interscience Publication, 1985) to give α,β-unsaturated ketones XXVII. By reaction with hydroxylamine, these give the corresponding oximes which can be converted into the 5-isoxazolyl derivatives by oxidative cyclization (J. Am. Chem. Soc. 1972, 94, 9128) (the meaning of R* thus corresponds to the meaning of a radical by which the heterocyclyl may be substituted).

It is also possible to convert the aldehydes XXV with alkoxymethylphosphonium salts in a manner known per se (J. March, “Advanced Organic Chemistry”, 3^(rd) edition, p. 864 ff., Wiley-Interscience Publication, 1985) into the corresponding enol ethers. Cleavage of these enol ethers analogously to processes known from the literature yield the acetaldehyde derivatives XXVIII. By bromination in the α-position these can be converted into the α-bromoacetaldehyde derivatives (Tetrahedron Lett. 1988, 29, 5893), which afford, by cyclization with amides, thioamides and amidines, oxazoles, thiazoles and imidazoles. Furthermore, the acetaldehyde derivatives XXVIII can be converted with dimethylformamide dimethyl acetal into corresponding enamines which can then be converted into isoxazoles or pyrazoles using hydroxylamines and hydrazines, respectively.

Furthermore, the aldehydes XXV can be converted into hydroxyketone derivatives by Aldol reaction with ketones. Subsequent oxidation leads to 1,3-diketones which can be converted into isoxazoles, pyrazoles or pyrimidines using hydroxylamine, hydrazines or amidines.

The aldehydes XXV can also be converted by methods known from the literature (Houben-Weyl, “Methoden der organischen Chemie”[Methods of Organic Chemistry], 4^(th) edition, Vol. E14b) into the corresponding diazo compounds XXIX. 1,3-dipolar cycloaddition to alkenes or alkynes and subsequent isomerization leads to pyrazolines or pyrazoles.

The aldehyde XXV can be prepared analogously to processes known from the literature, for example from the corresponding methyl compound XXX, by bromination, for example with N-bromosuccinimide or 1,3-dibromo-5,5-dimethylhydantoin, and subsequent oxidation (cf. Synth. Commun. 1992, 22, 1967-1971).

The oximes of the formula XXIV are advantageously obtained by reacting, in a manner known per se, aldehydes of the formula XXV with hydroxylamine (cf. J. March, “Advanced Organic Chemistry”, 3^(rd) edition, pp. 805-806, Wiley, New York, 1985).

The conversion of the oximes XXIV into the nitrites XXVI can also be carried out by processes known per se (cf. J. March, “Advanced Organic Chemistry”, 3^(rd) edition, pp. 931-932, Wiley, New York, 1985).

The nitrites of the formula XXVI can be converted in a manner known per se with hydroxylamine into the corresponding aldoximes XIX, converted with hydrogen sulfide into the thioamides XX or hydrolyzed to give the carboxylic acids XXI. The latter can also be obtained from the aldehydes XXV by oxidation (cf. J. March, “Advanced Organic Chemistry”, 3^(rd) edition, p. 629 ff., Wiley, New York, 1985).

The acyl halides XXII can be obtained analogously to standard processes from the corresponding carboxylic acids of the formula XXI.

The phosphorus-containing compounds of the formula IVδ are obtainable by reaction of compounds of the formula XXXII where L⁵=bromine, iodine, triflate and a corresponding substituted phosphorous acid or phosphonous acid in the presence of a transition metal catalyst, such as nickel or palladium, and, if appropriate, a base (cf., for example, T. Hirao et al., Synthesis 1981, 56.)

The compounds of the formula XXXII where L⁵=Br, I are obtained from the corresponding nitro compounds by reaction of the nitro group and subsequent Sandmeyer reaction. The compounds of the formula XXXII where L⁵=OSO₂CF₃ can be obtained by reacting the corresponding phenol with trifluoromethylsulfonyl chloride or trifluoromethylsulfonic anhydride.

The compounds of the formula IVδ where R¹, R²=C₁-C₆-alkoxy, C₁-C₆-alkylthio, C₁-C₆-alkylamino etc., can also be obtained by reaction of nucleophilically substitutable phosphorus compounds of the formula IVδ where L′, L″=a leaving group, such as halogen, C₁-C₆-alkoxy, etc., with suitable alcohols, amines or mercaptans, if appropriate in the presence of a base, (cf., for example, L. J. Kaplan, J.Org. Chem. 1979, 44, 2226; Houben-Weyl, “Methoden der organischen Chemie”[Methods of Organic Chemistry], Vol. XII/1, p. 423 ff.; R. Z. Greenley et al., J. Org. Chem. 1964, 29, 1009).

Compounds of the formula IVδ where L′, L″=halogen can be obtained by reaction of compounds of the formula IVδ where R¹, R²=OCH₃ with halogenating agents (cf. z. B. W. Althoff et al., Chem. Ber. 1978, 111, 1845).

Suitable halogenating agents are, inter alia, phosgene, thionyl chloride and thionyl bromide.

Compounds of the formula IVβ are furthermore obtainable by oxidation of compounds of the formula XXXIII.

Suitable oxidizing agents are, for example, potassium permanganate (cf., for example, Houben Weyl, “Methoden der Organischen Chemie”[Methods of Organic Chemistry], Vol. IV/1a, 1981, and Vol. VIII, 1952; E. I. Bengtsson, Acta Chem. Scand. 1953, 7, 774), chromium(VI) compounds (cf., for example, A. W. Singer et al., Org. Synth. Coll. Vol. III 1955, 740) or atmospheric oxygen in the presence of a catalyst such as, for example, cobalt or manganese (cf., for example, A. S. Hay et al., Can. J. Chem. 1965, 43, 1306).

The compounds of the formula XXXIII are obtainable by reaction of organometallic compounds of the formula XXXIV (where Met′=Li, Mg) with phosphorus compounds carrying nucleophilically replaceable groups (L=halogen, such as Cl, Br, alkoxy, etc.) (cf., for example, A. Berger et al., J. Org. Chem. 1951, 16, 1250; M. Sander, Chem. Ber. 1960, 93, 1220).

These compounds can also be obtained by oxidation of the corresponding phosphorus(III) compounds, which can be prepared analogously to the reaction shown above.

Suitable oxidizing agents are, for example, hydrogen peroxide, peroxyacetic acid, etc.

The compounds of the formula XXXIII (where R²=C₁-C₆-alkoxy, C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl, etc.) can furthermore be obtained by reacting a phosphorus compound of the formula XXXV with an alkyl halide (Arbuzov reaction).

Preferred alkyl halides are the corresponding bromides and iodides (cf., for example, B. A. Arbuzov, Pure Appl. Chem. 1964, 9, 307; G. M. Kosolapoff, Org. React. 1951, 6, 273).

In general, it is possible to introduce or synthesize the radical R³ at a suitable stage of the reaction sequence of the preparation of compounds of the formula I, where these reactions are described above or can be prepared analogously to known processes.

It may also be feasible to change the order of the reaction steps.

Furthermore, it is possible to modify the substituents R¹ and R² at a suitable stage of the reaction sequence. For example, the radicals R¹, R²=C₁-C₆-alkoxy can be converted by reaction with organometallic compounds into R¹, R²=C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl etc. Organometallic reagents which are suitable for this purpose are appropriate organolithium or organomagnesium compounds (cf., for example, Houben-Weyl, “Methoden der Organischen Chemie”[Methods of Organic Chemistry], Vol. E. 2, p. 38 ff., Wiley, New York).

Novel are the phosphorus-containing benzoic acid derivatives of the formula IV

where:

X is oxygen or sulfur;

R¹,R² are hydrogen, C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl, C₁-C₆-alkoxy, C₃-C₆-alkenyloxy, C₃-C₆-alkynyloxy, mercapto, C₁-C₆-alkylthio, C₃-C₆-alkenylthio, C₃-C₆-alkynylthio, amino, C₁-C₆-alkylamino, di(C₁-C₆-alkyl)amino, (C₁-C₆-alkoxy)(C₁-C₆-alkyl)amino, (C₃-C₆-alkenyl)(C₁-C₆-alkyl)amino, (C₃-C₆-alkynyl)(C₁-C₆-alkyl)amino, di(C₃-C₆-alkenyl)amino or di(C₃-C₆-alkynyl)amino, where the abovementioned alkyl, alkenyl or alkynyl radicals may be partially or fully halogenated and/or may carry one to three of the following groups:

nitro, cyano, C₁-C₄-alkoxy, C₁-C₄-alkylthio, C₁-C₄-alkylsulfinyl, C₁-C₄-alkylsulfonyl, di(C₁-C₄-alkyl)amino, C₁-C₄-alkylcarbonyl, C₁-C₄-alkoxycarbonyl,

are phenyl or heterocyclyl, where the two last-mentioned radicals for their part may be partially or fully halogenated and/or may carry one to three of the following groups:

nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy or C₁-C₄-alkoxycarbonyl;

are phenoxy which may by partially or fully halogenated and/or may carry one to three of the following groups: nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy or C₁-C₄-alkoxycarbonyl; or

R¹ and R² together form a —O—(CH₂)_(m)—O—, —O—(CH₂)_(m)—S—, —S—(CH₂)_(m)—S—, —NR⁵—(CH₂)_(m)—NR⁵—, —O—(CH₂)_(m)—NR⁵—, —S—(CH₂)_(m)—NR⁵—, —(CH₂)_(n)—O—, —(CH₂)_(n)—S— or —(CH₂)_(n)—NR⁵ chain which may carry one to three radicals from the following group:

halogen, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C_(l)-C₄-alkoxy, C₁-C₄-alkoxycarbonyl or phenyl which is unsubstituted or partially or fully halogenated and/or may carry one to three of the following groups: nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy or C₁-C₄-alkoxycarbonyl; or

R¹ and R² together form —(CH₂)_(p) chain which may be interrupted by oxygen, sulfur or NR⁵ and/or may carry one to three radicals from the following group:

halogen, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-alkoxycarbonyl or phenyl which is unsubstituted or partially or fully halogenated and/or may carry one to three of the following groups:

nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy or C₁-C₄-alkoxycarbonyl;

R³ is cyano, halogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy-C₁-C₆-alkyl, C₁-C₆-haloalkoxy-C₁-C₆-alkyl, C₁-C₆-alkylthio-C₁-C₆-alkyl, C₁-C₆-alkylsulfinyl-C₁-C₆-alkyl, C₁-C₆-alkylsulfonyl-C₁-C₆-alkyl, C₁-C₆-alkylcarbonyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₁-C₆-alkylthio, C₁-C₆-haloalkylthio, C₁-C₆-alkylsulfinyl, C₁-C₆-haloalkylsulfinyl, C₁-C₆-alkylsulfonyl, C₁-C₆-haloalkylsulfonyl, aminosulfonyl, C₁-C₆-alkylaminosulfonyl, di(C₁-C₆-alkyl)aminosulfonyl, (C₁-C₆-alkylsulfonyl)amino, (C₁-C₆-haloalkylsulfonyl)amino, N—(C₁-C₆-alkyl)—N—(C₁-C₆-alkylsulfonyl)amino, N—(C₁-C₆-alkyl)—N—(C₁-C₆-haloalkylsulfonyl)amino, —P(═X)R¹R², phenyl or heterocyclyl, where the two last-mentioned radicals may be partially or fully halogenated and/or may carry one to three of the following groups:

nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy or C₁-C₄-alkoxycarbonyl;

R⁴ is nitro, cyano, halogen, C₁-C₆-alkyl, C₁-C₆-alkoxy, C₁-C₆-alkylthio, C₁-C₆-alkylsulfinyl or C₁-C₆-alkylsulfonyl;

R⁵ is hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl or C₁-C₆-alkoxy;

l is 0, 1 or 2;

m is 2, 3 or 4;

n is 3, 4 or 5;

p is 4, 5 or 6;

R²⁶ is a radical which can be removed by hydrolysis.

Examples of radicals which can be removed by hydrolysis are alkoxy, phenoxy, alkylthio and phenylthio radicals, which may be unsubstituted or substituted; halides, heteroaryl radicals attached via nitrogen; amino and imino radicals which may be unsubstituted or substituted, etc.

Preference is given to phosphorus-containing benzoic acid derivatives of the formula IVα where L²=halogen (≡IV where R²⁶=halogen),

where the variables X, R¹ to R⁴ and l are as defined under the compounds of the formula IV. Hal is halogen, in particular chlorine or bromine.

Preference is also given to the phosphorus-containing benzoic derivatives of the formula IVβ (≡IV where R²⁶=hydroxyl),

where the variables X, R¹ to R⁴ and l are as defined under the compounds of the formula IV.

Preference is also given to the phosphorus-containing benzoic acid derivatives of the formula IVδ (≡IV where R²⁶=C₁-C₆-alkoxy),

where the variables X, R¹ to R⁴ and l are as defined under the compounds of the formula IV and

T is C₁-C₆-alkoxy.

The particularly preferred embodiments of the phosphorus-containing benzoic acid derivatives of the formulae IV, IVα where L²=halogen, IVβ and IVδ with respect to the variables X, R¹ to R⁴ and 1 correspond to those of the phosphorus-containing benzoyl derivatives of the formula I.

Particular preference is also given to the compounds of the formula IV where the variables have the following meanings:

R¹,R² are hydrogen, C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl, C₁-C₆-alkoxy, C₃-C₆-alkenyloxy, C₃-C₆-alkynyloxy, mercapto, C₁-C₆-alkylthio, C₃-C₆-alkenylthio, C₃-C₆-alkynylthio, amino, C₁-C₆-alkylamino or di-(C₁-C₆-alkyl)amino, where the alkyl, alkenyl or alkynyl radicals mentioned may be partially or fully halogenated and/or may carry one to three of the following groups:

nitro, cyano, C₁-C₄-alkoxy, C₁-C₄-alkylthio, C₁-C₄-alkylsulfonyl, di(C₁-C₄-alkyl)-amino, C₁-C₄-alkylcarbonyl, C₁-C₄-alkoxycarbonyl, phenyl or heterocyclyl, where the two lastmentioned radicals for their part may be partially or fully halogenated and/or may carry one to three of the following groups:

nitro, cyano, C₁—C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy or C₁-C₄-alkoxycarbonyl;

are phenoxy which may be partially or fully halogenated and/or may carry one to three of the following groups: nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy or C₁-C₄-alkoxycarbonyl; or

R¹ and R² together form a —O—(CH₂)_(m)—O—, —O—(CH₂)_(m)—S—, —S—(CH₂)_(m)—S—, —NR⁵—(CH₂)_(m)—NR⁵—, —O—(CH₂)_(m)—NR⁵— or —S—(CH₂)_(m)—NR⁵— chain which may carry one to three radicals from the following group:

halogen, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-alkoxycarbonyl or phenyl, which is unsubstituted or partially or fully halogenated and/or may carry one to three of the following groups:

nitro, cyano, C₁—C₄-alkyl, C₁—C₄-haloalkyl, C₁—C₄-alkoxy, C₁—C₄-haloalkoxy or C₁-C₄-alkoxycarbonyl;

R₃ is cyano, halogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkylcarbonyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₁-C₆-alkylthio, C₁-C₆-haloalkylthio, C₁-C₆-alkylsulfinyl, C₁-C₆-haloalkylsulfinyl, C₁-C₆-alkylsulfonyl, C₁-C₆-haloalkylsulfonyl, —P(═X)R¹R², phenyl or heterocyclyl, where the two lastmentioned radicals may be partially or fully halogenated and/or may carry one to three of the following groups:

nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy or C₁-C₄-alkoxycarbonyl;

R⁴ is nitro, cyano, halogen, C₁-C₆-alkyl, C₁-C₆-alkoxy, C₁-C₆-alkylthio, C₁-C₆-alkylsulfinyl or C₁-C₆-alkylsulfonyl;

R⁵ is hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl or C₁-C₆-alkoxy;

l is 0, 1 or 2;

m is 2, 3 or 4;

R²⁶ is a radical which can be removed by hydrolysis.

Especially preferred are the compounds of the formula IV where the variables have the following meanings:

R¹, R² are hydrogen, C₁-C₆-alkyl, C₁-C₆-alkoxy or C₁-C₆-alkylthio, where the alkyl radicals mentioned may be partially or fully halogenated and/or may carry one to three of the following groups: nitro, cyano, C₁-C₄-alkoxy, C₁-C₄-alkylthio, di-(C₁-C₄-alkyl)amino, C₁-C₄-alkylcarbonyl or C₁-C₄-alkoxycarbonyl;

R³ is cyano, halogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₁-C₆-alkylthio, C₁-C₆-haloalkylthio, C₁-C₆-alkylsulfinyl, C₁-C₆-haloalkylsulfinyl, C₁-C₆-alkylsulfonyl or C₁-C₆-haloalkylsulfonyl;

l is 0.

PREPARATION EXAMPLES 1. Synthesis of diethyl{3-chloro-4-[(2-hydroxy-4,4-dimethyl-6-oxocyclohex-1-en-1-yl)carbonyl]phenyl}phosphonate (Compound 3.1)

Step a) Diethyl(3-chloro-4-methylphenyl)phosphonate

A mixture of 32.0 g (0.127 mol) of 2-chloro-4-iodotoluene, 17.5 g (0.127 mol) of diethyl phosphite, 12.8 g (0.127 mol) of triethylamine and 14.7 g (0.0127 mol) of tetrakis(triphenylphosphine)palladium (0) in 200 ml of acetonitrile was refluxed for 5 hours. After cooling, the mixture was stirred into water and extracted with ethyl acetate. The organic phase was dried and concentrated and the residue was then distilled.

Yield: 23.4 g (70%); colorless oil

¹H NMR (CDCl₃): δ=7.88 (m,1H); 7.60 (m,1H); 7,52 (m,1H); 4.10 (m,4H); 2.40 (s,3H); 1.34 (t, 6H)

Step b) Diethyl(3-chloro-4-hydroxycarbonylphenyl)phosphonate (Compound 6.1)

At 80° C., a solution of 1.76 g (11 mmol) of potassium permanganate in 10 ml of water was added a little at a time to a solution of 1.0 g (3.81 mmol) of the product from step a) in 5 ml of pyridine. The mixture was stirred at room temperature for 6 hours, sodium carbonate solution was added and the precipitate was filtered off. The filtrate was acidified using hydrochloric acid and extracted with ethyl acetate.

Yield: 0.75 g (67%); colorless solid

¹H NMR (d⁶-DMSO) δ=13.8 (brd s, 1H); 7.90 (m,1H); 7.75 (m,2H); 4.06 (m,4H); 1.25 (t,6H)

Step c) Diethyl {3-chloro-4-[(2-hydroxy-4,4-dimethyl-6-oxo-cyclohex-1-en-1-yl)carbonyl]phenyl}phosphonate

A mixture of 0.65 g (2.2 mmol) of the product from step b), 0.45 g (2.2 mmol) of N,N-dicyclohexylcarbodiimide and 0.31 g of dimedone in 30 ml of acetonitrile was stirred at room temperature overnight. 0.45 g (4.4 mmol) of triethylamine and 0.2 ml of trimethylsilyl cyanide were then added, and the mixture was stirred at room temperature for a further 18 hours. The reaction mixture was poured into 50 ml each of ethyl acetate and 2% strength sodium carbonate solution and filtered. The aqueous phase was washed with diethyl ether and subsequently adjusted to a pH of 4-5 using hydrochloric acid. The mixture was extracted with ethyl acetate, the organic phase was dried and the solvent was removed.

Yield: 0.36 g (39%); red oil

¹H NMR (CDCl₃): δ=7.78 (m,2H); 7.28 (m,1H); 4.12 (m,4H); 2.65 (m,2H); 2.32 (m,2H); 1.32 (t,6H); 1.14 (s,6H).

2. Synthesis of diethyl {3-chloro-4-[(1-ethyl-5-hydroxy-1H-pyrazol-4-ylcarbonyl]phenyl}phosphonate (Compound 5.1)

At room temperature, a mixture of 1.0 g (3.4 mmol) of the product from Synthesis 1 step b), 0.71 g (3.4 mmol) of N,N-dicyclohexylcarbodiimide and 0.38 g (3.4 mmol) of 5-hydroxy-1-ethylpyrazole was stirred for 36 hours. The reaction mixture was poured into 50 ml each of ethyl acetate and 2% strength sodium carbonate solution, the organic phase was dried and the solvent was removed. The residue was chromatographed over silica gel using cyclohexane/ethyl acetate. The resulting O-acylated product (0.36 g) in 1,4-dioxane was then admixed with potassium carbonate and refluxed for 4 hours. The reaction mixture was poured into water and extracted with ethyl acetate. The aqueous phase was washed once with diethyl ether, adjusted to pH 4 using hydrochloric acid and extracted with ethyl acetate. The organic phase was dried and the solvent was removed.

Yield: 0.17 g; red oil

¹H NMR (CDCl₃): δ=7.95 (m,1H); 7.78 (m,1H); 7.55 (m,1H); 7.38 (s,1H); 4.40 (m,2H); 4.13 (m,4H); 1.44 (t,3H); 1.36 (t,6H)

In addition to the compounds of the formula I or IV described above, Tables 3 to 7 list other compounds which were prepared or are preparable in a similar manner:

TABLE 3

physical data mp [° C.]. No. R¹ R² R³ R⁴ _(l) R⁶ R⁷ R⁸ R⁹ R¹⁰ R¹¹ R¹² ¹H NMR [δppm] 3.1 OCH₂CH₃ OCH₂CH₃ Cl H(1 = O) OH H H CH₃ CH₃ H H 7.78(m.2H); 7.28(m.1H); 4.12(m.4H); 2.65(m.2H); 2.32(m.2H); 1.32(t.6H); 1.14(s.6H) 3.2 OCH₂CH₃ OCH₂CH₃ Cl H(1 = O) OH H H H H H H  97-98 3.3 CH₃ CH₃ Cl H(1 = O) OH H H CH₃ CH₃ H H 7.70(m.2H); 7.35(m.1H); 2.68(s.2H); 2.35(s.2H); 1.78(d.6H); 1.12(s.6H) 3.4 CH₃ CH₃ Cl H(1 = O) OH H H H H H H  60-62 3.5 CH₃ CH₃ Cl H(1 = O) OH CH₃ CH₃ ═O CH₃ CH₃  99-100 3.6 OCH₂CH₃ OCH₂CH₃ Cl H(1 = O) OH CH₃ CH₃ ═O CH₃ CH₃ 121-122

TABLE 4

physical data mp [° C.], No. R¹ R² R³ R⁴ _(l) R⁶ ¹H NMR [δppm] 4.1 OCH₂CH₃ OCH₂CH₃ Cl H(1 = O) SC₆H₅ 7.78(m.2H); 7.52(m.6H); 4.10(m.4H); 3.07(t.1H); 2.90(t.1H); 2.05(m.2H); 1.84(m.2H); 1.55(m.2H); 1.38(t.6H) 4.2 OCH₂CH₃ OCH₂CH₃ Cl H(1 = O) OH 150 4.3 CH₃ CH₃ Cl H(1 = O) OH 178-179

TABLE 5

physical data mp [° C.], No. R¹ R² R³ R⁴ _(l) R²⁰ R²¹ R²² ¹H NMR [δppm] 5.1 OCH₂CH₃ OCH₂CH₃ Cl H(1 = O) OH CH₂CH₃ H 7.95(m.1H); 7.78(m.1H); 7.55(m.1H); 7.38(s.1H); 4.40(m.2H); 4.13(m.4H); 1.44(t.3H); 1.36(t.6H) 5.2 OCH₂CH₃ OCH₂CH₃ Cl H(1 = O) OH CH₃ H 7.90(d.1H); 7.80(m.1H); 7.54(m.1H); 7.38(s.1H); 4.16(m.4H); 3.70(s.3H); 1.38(t.6H)

TABLE 6

physical data mp [° C.], No. R¹ R² R³ R⁴ _(l) R⁶ R⁷ R⁸ R⁹ R¹⁰ R¹¹ R¹² ¹H NMR [δppm] 6.1 CH₃ CH₃ Cl H(1 = O) OH H H H H H H 200-201 6.2 CH₃ CH₃ Cl H(1 = O) OH H H CH₃ CH₃ H H 161-162

TABLE 7 IV2

physical data mp [° C.], No. R¹ R² R³ R⁴ _(l) R²⁶ ¹H NMR [δ ppm] 7.1 OCH₂CH₃ OCH₂CH₃ Cl H(l═O) OH 13.8 (bs. 1H); 7.90 (m.1H);7.75 (m.2H); 4.06 (m.4H); 1.25 (t.6H) 7.2 CH₃ CH₃ Cl H(l═O) OH 7.84 (m.3H); 1.68 (d.6H)

The compounds of the formula I and their agriculturally useful salts are suitable, both in the form of isomer mixtures and in the form of the pure isomers, as herbicides. The herbicidal compositions comprising compounds of the formula I control vegetation on non-crop areas very efficiently, especially at high rates of application. They act against broad-leaved weeds and grass weeds in crops such as wheat, rice, maize, soya and cotton without causing any significant damage to the crop plants. This effect is mainly observed at low rates of application.

Depending on the application method in question, the compounds of the formula I, or herbicidal compositions comprising them, can additionally be employed in a further number of crop plants for eliminating undesirable plants. Examples of suitable crops are the following:

Allium cepa, Ananas comosus, Arachis hypogaea, Asparagus officinalis, Beta vulgaris spec. altissima, Beta vulgaris spec. rapa, Brassica napus var. napus, Brassica napus var. napobrassica, Brassica rapa var. silvestris, Camellia sinensis, Carthamus tinctorius, Carya illinoinensis, Citrus limon, Citrus sinensis, Coffea arabica (Coffea canephora, Coffea liberica), Cucumis sativus, Cynodon dactylon, Daucus carota, Elaeis guineensis, Fragaria vesca, Glycine max, Gossypium hirsutum, (Gossypium arboreum, Gossypium herbaceum, Gossypium vitifolium), Helianthus annuus, Hevea brasiliensis, Hordeum vulgare, Humulus lupulus, Ipomoea batatas, Juglans regia, Lens culinaris, Linum usitatissimum, Lycopersicon lycopersicum, Malus spec., Manihot esculenta, Medicago sativa, Musa spec., Nicotiana tabacum (N.rustica), Olea europaea, Oryza sativa, Phaseolus lunatus, Phaseolus vulgaris, Picea abies, Pinus spec., Pisum sativum, Prunus avium, Prunus persica, Pyrus communis, Ribes sylvestre, Ricinus communis, Saccharum officinarum, Secale cereale, Solanum tuberosum, Sorghum bicolor (s. vulgare), Theobroma cacao, Trifolium pratense, Triticum aestivum, Triticum durum, Vicia faba, Vitis vinifera and Zea mays.

In addition, the compounds of the formula I may also be used in crops which tolerate the action of herbicides owing to breeding, including genetic engineering methods.

The compounds of the formula I, or the compositions comprising them, can be used for example in the form of ready-to-spray aqueous solutions, powders, suspensions, also highly-concentrated aqueous, oily or other suspensions or dispersions, emulsions, oil dispersions, pastes, dusts, materials for broadcasting, or granules, by means of spraying, atomizing, dusting, spreading or watering. The use forms depend on the intended purpose; in any case, they should guarantee the finest possible distribution of the active ingredients according to the invention.

The herbicidal compositions comprise a herbicidally effective amount of at least one compound of the formula I or an agriculturally useful salt of I, and auxiliaries which are customary for the formulation of crop protection agents.

Suitable as inert auxiliaries are essentially the following:

mineral oil fractions of medium to high boiling point, such as kerosene and diesel oil, furthermore coal tar oils and oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons, e.g. paraffin, tetrahydronaphthalene, alkylated naphthalenes and their derivatives, alkylated benzenes and their derivatives, alcohols such as methanol, ethanol, propanol, butanol and cyclohexanol, ketones such as cyclohexanone, strongly polar solvents, e.g. amines such as N-methylpyrrolidone, and water.

Aqueous use forms can be prepared from emulsion concentrates, Asuspensions, pastes, wettable powders or water-dispersible granules by adding water. To prepare emulsions, pastes or oil dispersions, the phosphorus-containing benzoyl derivatives of the formula I, either as such or dissolved in an oil or solvent, can be homogenized in water by means of a wetting agent, tackifier, dispersant or emulsifier. Alternatively, it is also possible to prepare concentrates comprising active ingredient, wetting agent, tackifier, dispersant or emulsifier and, if desired, solvent or oil, which are suitable for dilution with water.

Suitable surfactants are the alkali metal salts, alkaline earth metal salts and ammonium salts of aromatic sulfonic acids, e.g. ligno-, phenol-, naphthalene- and dibutylnaphthalenesulfonic acid, and of fatty acids, alkyl- and alkylarylsulfonates, alkyl sulfates, lauryl ether sulfates and fatty alcohol sulfates, and salts of sulfated hexa-, hepta- and octadecanols, and also of fatty alcohol glycol ethers, condensates of sulfonated naphthalene and its derivatives with formaldehyde, condensates of naphthalene or of the naphthalenesulfonic acids with phenol and formaldehyde, polyoxyethylene octylphenol ether, ethoxylated isooctyl-, octyl- or nonylphenol, alkylphenyl or tributylphenyl polyglycol ether, alkylaryl polyether alcohols, isotridecyl alcohol, fatty alcohol/ethylene oxide condensates, ethoxylated castor oil, polyoxyethylene alkyl ethers or polyoxypropylene alkyl ethers, lauryl alcohol polyglycol ether acetate, sorbitol esters, lignin-sulfite waste liquors or methylcellulose.

Powders, materials for scattering and dusts can be prepared by mixing or grinding the active ingredients together with a solid carrier.

Granules, e.g. coated granules, impregnated granules and homogeneous granules, can be prepared by binding the active ingredients to solid carriers. Solid carriers are mineral earths such as silicas, silica gels, silicates, talc, kaolin, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate and magnesium oxide, ground synthetic materials, fertilizers such as ammonium sulfate, ammonium phosphate, ammonium nitrate and ureas, and products of vegetable origin, such as cereal meal, tree bark meal, wood meal and nutshell meal, cellulose powders, or other solid carriers.

The concentrations of the compounds of the formula I in the ready-to-use preparations can be varied within wide ranges. In general, the formulations comprise approximately from 0.001 to 98% by weight, preferably 0.01 to 95% by weight of at least one active ingredient. The active ingredients are employed in a purity of from 90% to 100%, preferably 95% to 100% (according to NMR spectrum).

The formulation examples below illustrate the preparation of such compositions:

I. 20 parts by weight of the compound No. 3.3 are dissolved in a mixture composed of 80 parts by weight of alkylated benzene, 10 parts by weight of the adduct of from 8 to 10 mol of ethylene oxide to 1 mol of oleic acid N-monoethanol-amide, 5 parts by weight of calcium dodecylbenzenesulfonate and 5 parts by weight of the adduct of 40 mol of ethylene oxide to 1 mol of castor oil. Pouring the solution into 100,000 parts by weight of water and finely distributing it therein gives an aqueous dispersion which comprises 0.02% by weight of the active ingredient.

iii. 20 parts by weight of the compound No. 3.3 are dissolved in a mixture composed of 40 parts by weight of cyclohexanone, 30 parts by weight of isobutanol, 20 parts by weight of the adduct of 7 mol of ethylene oxide to 1 mol of isooctyl-phenol and 10 parts by weight of the adduct of 40 mol of ethylene oxide to 1 mol of castor oil. Pouring the solution into 100,000 parts by weight of water and finely distributing it therein gives an aqueous dispersion which comprises 0.02% by weight of the active ingredient.

II. 20 parts by weight of the compound No. 3.3 are dissolved in a mixture composed of 25 parts by weight of cyclohexanone, 65 parts by weight of a mineral oil fraction of boiling point 210 to 280° C. and 10 parts by weight of the adduct of 40 mol of ethylene oxide to 1 mol of castor oil. Pouring the solution into 100,000 parts by weight of water and finely distributing it therein gives an aqueous dispersion which comprises 0.02% by weight of the active ingredient.

IV. 20 parts by weight of the compound No. 3.3 are mixed thoroughly with 3 parts by weight of sodium diisobutylnaphthalenesulfonate, 17 parts by weight of the sodium salt of a lignosulfonic acid from a sulfite waste liquor and 60 parts by weight of pulverulent silica gel, and the mixture is ground in a hammer mill. Finely distributing the mixture in 20,000 parts by weight of water gives a spray mixture which comprises 0.1% by weight of the active ingredient.

V. 3 parts by weight of the compound No. 3.3 are mixed with 97 parts by weight of finely divided kaolin. This gives a dust which comprises 3% by weight of the active ingredient.

VI. 20 parts by weight of the compound No. 3.3 are mixed intimately with 2 parts by weight of calcium dodecylbenzenesulfonate, 8 parts by weight of fatty alcohol polyglycol ether, 2 parts by weight of the sodium salt of a phenol/urea/formaldehyde condensate and 68 parts by weight of a paraffinic mineral oil. This gives a stable oily dispersion.

VII. 1 part by weight of the compound No. 3.3 is dissolved in a mixture composed of 70 parts by weight of cyclohexanone, 20 parts by weight of ethoxylated isooctylphenol and 10 parts by weight of ethoxylated castor oil. This gives a stable emulsion concentrate.

VIII. 1 part by weight of the compound No. 3.3 is dissolved in a mixture composed of 80 parts by weight of cyclohexanone and 20 parts by weight of Wettol® EM 31 (=nonionic emulsifier based on ethoxylated castor oil). This gives a stable emulsion concentrate.

The compounds of the formula I or the herbicidal compositions can be appled pre- or post-emergence. If the active ingredients are less well tolerated by certain crop plants, application techniques may be used in which the herbicidal compositions are sprayed, with the aid of the spraying equipment, in such a way that as far as possible they do not come into contact with the leaves of the sensitive crop plants, while the active ingredients reach the leaves of undesirable plants growing underneath, or the bare soil surface (post-directed, lay-by).

The rates of application of the compound of the formula I are from 0.001 to 3.0, preferably 0.01 to 1.0, kg/ha of active substance (a.s.), depending on the control target, the season, the target plants and the growth stage.

To widen the spectrum of action and to achieve synergistic effects, the phosphorus-containing benzoyl derivatives of the formula I may be mixed with a large number of representatives of other herbicidal or growth-regulating active ingredient groups and then applied concomitantly. Suitable components for mixtures are, for example, 1,2,4-thiadiazoles, 1,3,4-thiadiazoles, amides, amino-phosphoric acid and its derivatives, aminotriazoles, anilides, aryloxy-/heteroaryloxyalkanoic acids and their derivatives, benzoic acid and its derivatives, benzothiadiazinones, 2-aroyl-1,3-cyclohexanediones, hetaryl aryl ketones, benzylisoxazolidinones, meta-CF₃-phenyl derivatives, carbamates, quinolinecarboxylic acid and its derivatives, chloroacetanilides, cyclohexenone oxime ether derivatives, diazines, dichloropropionic acid and its derivatives, dihydrobenzofurans, dihydrofuran-3-ones, dinitroanilines, dinitrophenols, diphenyl ethers, dipyridyls, halocarboxylic acids and their derivatives, ureas, 3-phenyluracils, imidazoles, imidazolinones, N-phenyl-3,4,5,6-tetrahydro-phthalimides, oxadiazoles, oxiranes, phenols, aryloxy- and hetaryloxyphenoxypropionic esters, phenylacetic acid and its derivatives, phenylpropionic acid and its derivatives, pyrazoles, phenylpyrazoles, pyridazines, pyridinecarboxylic acid and its derivatives, pyrimidyl ethers, sulfonamides, sulfonylureas, triazines, triazinones, triazolinones, triazolecarboxamides and uracils.

It may furthermore be advantageous to apply the compounds of the formula I, alone or in combination with other herbicides, or in the form of a mixture with other crop protection agents, for example together with agents for controlling pests or phytopathogenic fungi or bacteria. Also of interest is the miscibility with mineral salt solutions, which are employed for treating nutritional and trace element deficiencies.

Non-phytotoxic oils and oil concentrates may also be added.

USE EXAMPLES

The herbicidal activity of the phosphorus-containing benzoyl derivatives of the formula I was demonstrated by the following greenhouse experiments:

The culture containers used were plastic flowerpots containing loamy sand with approximately 3.0% of humus as the substrate. The seeds of the test plants were sown separately for each species.

For the pre-emergence treatment, the active ingredients, which had been suspended or emulsified in water, were applied directly after sowing by means of finely distributing nozzles. The containers were irrigated gently to promote germination and growth and subsequently covered with transparent plastic hoods until the plants had rooted. This cover causes uniform germination of the test plants, unless this was adversely affected by the active ingredients.

For the post-emergence treatment, the test plants were first grown to a height of 3 to 15 cm, depending on the plant habit, and only then treated with the active compounds which had been suspended or emulsified in water. For this purpose, the test plants were either sown directly and grown in the same containers, or they were first grown separately as seedlings and transplanted into the test containers a few days prior to treatment. The rate of application for the post-emergence treatment was 0.5 or 0.25 kg/ha of a.s. (active substance).

Depending on the species, the plants were kept at 10-25° C. or 20-35° C. The test period extended over 2 to 4 weeks. During this time, the plants were tended, and their response to the individual treatments was evaluated.

Evaluation was carried out using a scale from 0 to 100. 100 means no emergence of the plants, or complete destruction of at least the aerial parts, and 0 means no damage, or normal course of growth.

The plants used in the greenhouse experiments belonged to the following species:

338 Scientific name English name Chenopodium album lambsquarters (goosefoot) Echinochloa crus-galli barnyardgrass Setaria faberi giant foxtail Setaria viridis green foxtail Solanum nigrum black nightshade

The compounds 3.4, applied post-emergence, showed very good activity against the abovementioned harmful plants at rates of application of 0.5 and 0.25 kg/ha, respectively. 

We claim:
 1. Phosphorus-containing benzoyl derivatives of the formula I

in which: X is oxygen or sulfur; R¹, R² are hydrogen, C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl, hydroxyl, C₁-C₆-alkoxy, C₃-C₆-alkenyloxy, C₃-C₆-alkynyloxy, mercapto, C₁-C₆-alkylthio, C₃-C₆-alkenylthio, C₃-C₆-alkynylthio, amino, C₁-C₆-alkylamino, di(C₁-C₆-alkyl)amino, (C₁-C₆-alkoxy)(C₁-C₆-alkyl)amino, (C₃-C₆-alkenyl)(C₁-C₆-alkyl)amino, (C₃-C₆-alkynyl)(C₁-C₆-alkyl)amino, di(C₃-C₆-alkenyl)amino or di(C₃-C₆-alkynyl)amino, where the abovementioned alkyl, alkenyl or alkynyl radicals may be partially or fully halogenated and/or may carry one to three of the following groups: nitro, cyano, C₁-C₄-alkoxy, C₁-C₄-alkylthio, C₁-C₄-alkylsulfinyl, C₁-C₄-alkylsulfonyl, di(C₁-C₄-alkyl)amino, C₁-C₄-alkylcarbonyl, C₁-C₄-alkoxycarbonyl, phenyl or heterocyclyl, where the two last-mentioned radicals for their part may be partially or fully halogenated and/or may carry one to three of the following groups: nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy or C₁-C₄-alkoxycarbonyl; are phenyl or phenoxy which may by partially or fully halogenated and/or may carry one to three of the following groups: nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy or C₁-C₄-alkoxycarbonyl; or R¹ and R² together form an —O—(CH₂)_(m)—O—, —O—(CH₂)_(m)—S—, —S—(CH₂)_(m)—S—, —NR⁵—(CH₂)_(m)—NR⁵—, —O—(CH₂)_(m)—NR⁵—, —S—(CH₂)_(m)—NR⁵—, —(CH₂)_(n)—O—, —(CH₂)_(n)—S— or —(CH₂)_(n)—NR⁵ chain which may carry one to three radicals from the following group: halogen, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-alkoxycarbonyl or phenyl which is unsubstituted or partially or fully halogenated and/or may carry one to three of the following groups: nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy or C₁-C₄-alkoxycarbonyl; or R¹ and R² together form a —(CH₂)_(p) chain which may be interrupted by oxygen, sulfur or NR⁵ and/or may carry one to three radicals from the following group: halogen, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-alkoxycarbonyl or phenyl which is unsubstituted or partially or fully halogenated and/or may carry one to three of the following groups: nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy or C₁-C₄-alkoxycarbonyl; R³ is hydrogen, nitro, cyano, halogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy-C₁-C₆-alkyl, C₁-C₆-haloalkoxy-C₁-C₆alkyl, C₁-C₆-alkylthio-C₁-C₆-alkyl, C₁-C₆-alkylsulfinyl-C₁-C₆-alkyl, C₁-C₆-alkylsulfonyl-C₁-C₆-alkyl, C₁-C₆-alkylcarbonyl, C₁-C₆-alkoxycarbonyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₁-C₆-alkylthio, C₁-C₆-haloalkylthio, C₁-C₆-alkylsulfinyl, C₁-C₆-haloalkylsulfinyl, C₁-C₆-alkylsulfonyl, C₁-C₆-haloalkylsulfonyl, aminosulfonyl, C₁-C₆-alkylaminosulfonyl, di(C₁-C₆-alkyl)aminosulfonyl, (C₁-C₆-alkylsulfonyl)amino, (C₁-C₆-haloalkylsulfonyl)amino, N—(C₁-C₆-alkyl)—N—(C₁-C₆-alkylsulfonyl)amino, N—(C₁-C₆-alkyl)-N—(C₁-C₆-haloalkylsulfonyl)amino, —P(═X)R¹R², phenyl or heterocyclyl, where the two last-mentioned radicals may be partially or fully halogenated and/or may carry one to three of the following groups: nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy or C₁-C₄-alkoxycarbonyl; R⁴ is nitro, cyano, halogen, C₁-C₆-alkyl, C₁-C₆-alkoxy, C₁-C₆-alkylthio, C₁-C₆-alkylsulfinyl or C₁-C₆-alkylsulfonyl; R⁵ is hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl or C₁-C₆-alkoxy; l is 0, 1 or 2; m is 2, 3 or 4; n is 3, 4 or 5; p is 4, 5 or 6; Q is a radical of the formula Q¹

R⁶ is hydroxyl, mercapto, halogen, OR¹³, SR¹³, SOR¹⁴, SO₂R¹⁴, OSO₂R¹⁴, POR¹⁵R¹⁶, OPR¹⁵R¹⁶, OPOR¹⁵R¹⁶, OPSR¹⁵R¹⁶, NR¹⁷R¹⁸, ONR¹⁸R¹⁹, N-bonded heterocyclyl or O—(N-bonded heterocyclyl), where the heterocyclyl radical of the two last-mentioned substituents may be partially or fully halogenated and/or may carry one to three of the following radicals: nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy or C₁-C₄-haloalkoxy; R⁷, R⁹, R¹¹ are hydrogen, nitro, halogen, cyano, C₁-C₆-alkyl, C₁-C₆-haloalky, di(C₁-C₆-alkoxy)methyl, di(C₁-C₆-alkylthio)methyl, (C₁-C₆-alkoxy)(C₁-C₆-alkylthio)methyl, hydroxyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₁-C₆-alkoxycarbonyloxy, C₁-C₆-alkylthio, C₁-C₆-haloalkylthio, C₁-C₆-alkylsulfinyl, C₁-C₆-haloalkylsulfinyl, C₁-C₆-alkylsulfonyl, C₁-C₆-haloalkylsulfonyl, C₁-C₆-alkylcarbonyl, C₁-C₆-haloalkylcarbonyl, C₁-C₆-alkoxycarbonyl or C₁-C₆-haloalkoxycarbonyl; R⁸, R¹⁰, R¹² are hydrogen, C₁-C₆-alkyl, C₁-C₆-alkoxy, C₁-C₆-alkylthio or C₁-C₆-alkoxycarbonyl; or R⁷ and R⁸ or R⁹ and R¹⁰ or R¹¹ and R¹² together form an —O—(CH₂)_(u)—O—, —O—(CH₂)_(u)—S—, —S—(CH₂)_(u)—S—, —O—(CH₂)_(v)— or —S—(CH₂)_(v) chain which may be substituted by one to three radicals from the following group: halogen, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl or C₁-C₄-alkoxycarbonyl; or R⁷ and R⁸ or R⁹ and R¹⁰ or R¹¹ and R¹² together form a —(CH₂)_(w) chain which may be interrupted by oxygen or sulfur and/or may be substituted by one to four radicals from the following group: halogen, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl or C₁-C₄-alkoxycarbonyl; or R⁷ and R⁸ or R⁹ and R¹⁰ or R¹¹ and R¹² together form a methylidene group which may be substituted by one to two radicals from the following group: halogen, hydroxyl, formyl, cyano, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₁-C₆-alkylthio, C₁-C₆-haloalkylthio, C₁-C₆-alkylsulfinyl, C₁-C₆-haloalkylsulfinyl, C₁-C₆-alkylsulfonyl or C₁-C₆-haloalkylsulfonyl; or R⁷ and R⁸ or R⁹ and R¹⁰ or R¹¹ and R¹² together with the carbon to which they are attached form a carbonyl group; or R⁷ and R⁹ or R⁹ and R¹¹ or R⁷ and R¹¹ together form a —(CH₂)_(v) chain which may be substituted by one to three radicals from the following group: halogen, C₁-C₆-alkyl, C₁-C₆-alkoxy, hydroxyl or C₁-C₆-alkoxycarbonyl; R¹³ is C₁-C₆-alkyl, C₃-C₆-alkenyl, C₃-C₆-haloalkenyl, C₃-C₆-alkynyl, C₃-C₆-haloalkynyl, C₃-C₆cycloalkyl, C₁-C₂₀-alkylcarbonyl, C₂-C₆-alkenylcarbonyl, C₂-C₆-alkynylcarbonyl, C₃-C₆-cycloalkylcarbonyl, C₁-C₆-alkylaminocarbonyl, C₁-C₆-alkylcarbonyl-C₁-C₆-alkyl or C₁-C₆-alkoxyimino-C₁-C₆-alkyl, where the abovementioned alkyl and cycloalkyl radicals may be partially or fully halogenated and/or may carry one to three of the following groups: cyano, C₁-C₄-alkoxy, C₁-C₄-alkylthio, di(C₁-C₄-alkyl)amino, C₁-C₄-alkylcarbonyl, C₁-C₄-alkoxycarbonyl, C₁-C₄-alkoxy-C₁-C₄-alkoxycarbonyl, di(C₁-C₄-alkyl)amino-C₁-C₄-alkoxycarbonyl, hydroxycarbonyl, C₁-C₄-alkylaminocarbonyl, di(C₁-C₄-alkyl)-aminocarbonyl, aminocarbonyl, C₁-C₄-alkylcarbonyloxy or C₃-C₆-cycloalkyl; is phenyl, heterocyclyl, phenyl-C₁-C₆-alkyl, heterocyclyl-C₁-C₆-alkyl, phenylcarbonyl, heterocyclylcarbonyl, phenylaminocarbonyl or heterocyclylaminocarbonyl, where the phenyl and the heterocyclyl radical of the 8 last-mentioned substituents may be partially or fully halogenated and/or may carry one to three of the following radicals: nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy or C₁-C₄-haloalkoxy; R¹⁴, R¹⁵, R¹⁶ are C₁-C₆-alkyl, C₃-C₆-alkenyl, C₃-C₆-haloalkenyl, C₃-C₆-alkynyl, C₃-C₆-haloalkynyl, C₃-C₆-cycloalkyl, hydroxyl, C₁-C₆-alkoxy, amino, C₁-C₆-alkylamino, C₁-C₆-haloalkylamino, di(C₁-C₆-alkyl)amino or di(C₁-C₆-haloalkyl)amino, where the abovementioned alkyl, cycloalkyl and alkoxy radicals may be partially or fully halogenated and/or may carry one to three of the following groups: cyano, C₁-C₄-alkoxy, C₁-C₄-alkylthio, di(C₁-C₄-alkyl)amino, C₁-C₄-alkylcarbonyl or C₁-C₄-alkoxycarbonyl; are phenyl, heterocyclyl, phenoxy or heterocyclyloxy, where the phenyl and the heterocyclyl radical of the last-mentioned substituents may be partially or fully halogenated and/or may carry one to three of the following radicals: nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy or C₁-C₄-haloalkoxy; R¹⁷ is C₁-C₆-alkyl, C₃-C₆-alkenyl, C₃-C₆-haloalkenyl, C₃-C₆-alkynyl, C₃-C₆-haloalkynyl, C₃-C₆-cycloalkyl, hydroxyl, C₁-C₆-alkoxy, C₃-C₆-alkenyloxy or C₃-C₆-alkynyloxy, where the abovementioned alkyl, cycloalkyl and alkoxy radicals may be partially or fully halogenated and/or may carry one to three radicals from the following group: cyano, C₁-C₄-alkoxy, C₁-C₄-alkylthio or di(C₁-C₄-alkyl)amino; is phenyl, heterocyclyl, phenyl-C₁-C₆-alkyl or heterocyclyl-C₁-C₆-alkyl, where the phenyl or heterocyclyl radical of the four last-mentioned substituents may be partially or fully halogenated and/or may carry one to three of the following radicals: nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy or C₁-C₄-haloalkoxy; R¹⁸, R¹⁹ are C₁-C₆-alkyl, C₃-C₆-alkenyl, C₃-C₆-alkynyl or C₁-C₆-alkylcarbonyl; u is from 2 to 4; v is from 1 to 5; w is from 2 to 5; or an agriculturally useful salt thereof.
 2. A phosphorus-containing benzoyl derivative of the formula I as claimed in claim 1 where X═O and R³ is attached in position 4, R⁴ _(l) is attached in position 5 and “P(═X)R¹R²” is attached in position 2 (I1).


3. A phosphorus-containing benzoyl derivative of the formula I as claimed in claim 1 where X═O and R³ is attached in position 2, R⁴ _(l) is attached in position 5 and “P(═X)R¹R²” is attached in position 4 (I2).


4. A phosphorus-containing benzoyl derivtive of the formula I as claimed in claim 1 where R¹, R² are hydrogen, hydroxyl, C₁-C₆-alkyl, C₁-C₆-alkoxy, C₁-C₆-alkylthio, di-(C₁-C₆-alkyl)amino, where the alkyl radicals of the four lastmentioned substituents may be partially or fully halogenated and/or may carry one to three of the following groups: nitro, cyano, C₁-C₄-alkoxy, C₁-C₄-alkylsulfonyl or C₁-C₄-alkoxycarbonyl; or R¹ and R² together form a —O—(CH₂)_(m)—O—, —O—(CH₂)_(m)—S—, —S—(CH₂)_(m)—S—, —NR⁵—(CH₂)_(m)—NR⁵—, —O—(CH₂)_(m)—NR⁵—, —S—(CH₂)_(m)—NR⁵— or —(CH₂)_(p)— chain which may carry one to three radicals from the following group: halogen, cyano, C₁-C₄-alkyl or C₁-C₄-alkoxycarbonyl.
 5. A phosphorus-containing benzoyl derivative of the formula I as claimed in claim 1 where R³ is nitro, halogen, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₁-C₄-alkylthio, C₁-C₄-alkylsulfonyl, C₁-C₄-haloalkylsulfonyl, —P(═O)(CH₃)₂, —P(═O)(CH₂CH₃)₂, —P(═O)(OCH₃)₂ or —P(═O)(OCH₂CH₃)₂.
 6. A process for preparing, compounds of the formula Ia (≡I where Q=Q¹) where R⁶=halogen as claimed in claim 1, which comprises reacting a corresponding phosphorus-containing benzoyl derivative of the formula Ia (≡I where Q=Q¹) where R⁶=hydroxyl

with a halogenating agent.
 7. A process for preparing compounds of the formula Ia (≡I where Q=Q¹) where R⁶=OR¹³, OSO₂R¹⁴, OPR¹⁵R¹⁶, OPOR¹⁵R¹⁶ or OPSR¹⁵R¹⁶ as claimed in claim 1, which comprises reacting a corresponding phosphorus-containing benzoyl derivative of the formula Ia (≡I where Q=Q¹) where R⁶=hydroxyl

with a compound of the formula IIα, IIβ, IIγ, IIδ or IIε,

where the variables R¹³ to R¹⁶ are as defined in claim 1 and L¹ is a nucleophilically replaceable leaving group.
 8. A process for preparing compounds of the formula Ia (≡I where Q=Q¹) where R=OR¹³, SR¹³, POR¹⁵R¹⁶, NR¹⁷R¹⁸, ONR¹⁸R¹⁹, N-bonded heterocyclyl or O—N-bonded heterocyclyl as claimed in claim 1, which comprises reacting a corresponding phosphorus-containing benzoyl derivative of the formula Ia (≡I where Q=Q¹) where R⁶=halogen or OSO₂R¹⁴

with a compound of the formula IIIα, IIIβ, IIIγ, IIIδ or IIIε, IIIη or IIIΘ

where the variables R¹³ to R¹⁹ are as defined in claim 1, if appropriate in the presence of a base.
 9. A process for preparing compounds of the formula Ia (≡I where Q=Q¹) where R⁶=SOR¹⁴, SO₂R¹⁴ as claimed in claim 1, which comprises reacting a corresponding phosphorus-containing benzoyl derivative of the formula Ia (≡I where Q=Q¹) where R⁶=SR¹⁴

with an oxidizing agent.
 10. A process for preparing compounds of the formula Ia (≡I where Q=Q¹) where R⁶=hydroxyl as claimed in claim 1, which comprises acylating a cyclohexanedione of the formula V

where the variables R⁷ to R¹² are as defined in claim 1 with an activated phosphorus-containing benzoic acid of the formula IVα or a phosphorus-containing benzoic acid of the formula IVβ

where the variables X, R¹ to R⁴ and l are as defined in claim 1 and L² is a nucleophilically displaceable leaving group, and rearranging the acylation product, if appropriate in the presence of a catalyst.
 11. A composition, comprising a herbicidally effective amount of at least one phosphorus-containing benzoyl derivative of the formula I or an agriculturally useful salt of I as claimed in claim 1 and auxiliaries which are customarily used for formulating crop protection agents.
 12. A process for preparing compositions as claimed in claim 11, which comprises mixing a herbicidally effective amount of at least one phosphoris-containing benzoyl derivative of the formula I or of an agriculturally useful salt of I as claimed in claim 1 and auxiliaries which are customarily used for formulating crop protection agents.
 13. A method for controlling undesirable vegetation, which comprises allowing a herbicidally effective amount of at least one phosphorus-containing benzoyl derivative of the formula I or an agriculturally useful salt of I as claimed in claim 1 to act on plants, their habitat and/or on seed. 